公开(公告)号：JP2006206597A

公开(公告)日：2006-08-10

申请号：JP2006052376

申请日：2006-02-28

Applicant: Abbott Lab ,  アボット・ラボラトリーズAbbott Laboratories

Inventor： STUK TIMOTHY L ,  KERDESKY FRANCIS A J ,  LIJEWSKI LINDA M ,  NORBECK DANIEL W ,  SCARPETTI DAVID ,  TIEN JIEN-HEH J ,  ALLEN MICHAEL S ,  LANGRIDGE DENTON C ,  MELCHER LAURA ,  RENO DANIEL S ,  SHAM HING LEUNG ,  ZHAO CHEN ,  HAIGHT ANTHONY R ,  LEANNA M ROBERT ,  MORTON HOWARD E ,  ROBBINS TIMOTHY A ,  SOWIN THOMAS J

IPC: C07C215/28 ,  C07B61/00 ,  C07C213/00 ,  C07C225/14 ,  C07C225/16 ,  C07C227/18 ,  C07C229/36 ,  C07C231/12 ,  C07C233/35 ,  C07C251/38 ,  C07C251/40 ,  C07C255/27 ,  C07C255/42 ,  C07C269/06 ,  C07C271/20 ,  C07D209/44 ,  C07D221/14

CPC classification number: C07D221/14 ,  C07B2200/07 ,  C07C213/00 ,  C07C215/28 ,  C07C225/16 ,  C07C251/40 ,  C07C255/42 ,  C07C269/06 ,  C07C271/20 ,  C07D209/44 ,  C07C215/08

Abstract: PROBLEM TO BE SOLVED: To provide a substituted 2,5-diamino-3-hydroxyhexane useful for producing HIV protease inhibitors, and to provide a method for producing the compound.
SOLUTION: The substituted 2,5-diamino-3-hydroxyhexane useful for producing HIV protease inhibitors is represented by general formula I.
COPYRIGHT: (C)2006,JPO&NCIPI

Abstract translation: 待解决的问题：提供可用于产生HIV蛋白酶抑制剂的取代的2,5-二氨基-3-羟基己烷，并提供一种生产该化合物的方法。 解决方案：用于生产HIV蛋白酶抑制剂的取代的2,5-二氨基-3-羟基己烷由通式I表示。（C）2006，JPO和NCIPI

公开(公告)号：JP2011088904A

公开(公告)日：2011-05-06

申请号：JP2010267057

申请日：2010-11-30

Applicant: Abbott Lab ,  アボット・ラボラトリーズAbbott Laboratories

Inventor： ALLEN MICHAEL S ,  PREMCHANDRAN RAMIYA H ,  CHANG SOU-JEN ,  CONDON STEPHEN ,  DEMATTEI JOHN J ,  KING STEVEN A ,  KOLACZKOWSKI LAWRENCE ,  MANNA SUKUMAR ,  NICHOLS PAUL J ,  PATEL HEMANT H ,  PATEL SUBHASH R ,  PLATA DANIEL J ,  ERIK J SUTOONAA ,  TIEN JIEN-HEH J ,  WITTENBERGER STEVEN J

IPC: C07D215/14 ,  C07B61/00 ,  C07C68/06 ,  C07D215/18 ,  C07D401/12 ,  C07H17/08

CPC classification number: C07D215/14 ,  C07C68/06 ,  C07C69/96

Abstract: PROBLEM TO BE SOLVED: To provide a method for preparing quinoline-substituted carbonate and carbamate compounds which are important intermediates in the synthesis of a 6-O-substituted macrolide antibiotic material.
SOLUTION: The carbonate or carbamate derivative expressed by the formula: R
1 -CH=CHCH
2 OC(O)-X-R
2 (I) is obtained by coupling a haloquinoline with propargyl alcohol in the presence of a base and a palladium-based catalyst to form an alkynol, reducing it to make an alkenol and then reacting it with an acylation reagent.
COPYRIGHT: (C)2011,JPO&INPIT

Abstract translation: 待解决的问题：提供一种制备喹啉取代的碳酸酯和氨基甲酸酯化合物的方法，其是合成6-O-取代的大环内酯类抗生素材料的重要中间体。 解决方案：由下式表示的碳酸酯或氨基甲酸酯衍生物：R 1 = CHCH 2 S（O）-XR 2 S / （I）通过在碱和钯基催化剂的存在下将卤代喹啉与炔丙醇偶联以形成炔醇，将其还原成烯醇，然后使其与酰化试剂反应而获得。 版权所有（C）2011，JPO＆INPIT

公开(公告)号：DK1007517T3

公开(公告)日：2004-02-09

申请号：DK98942099

申请日：1998-08-18

Applicant: ABBOTT LAB

Inventor： ALLEN MICHAEL S

IPC: C07D277/20 ,  C07D277/22 ,  C07D277/24 ,  C07D277/32

Abstract: The present invention discloses a process for the preparation of a hydroxymethylthiazole compound having formula 3: The process of the invention comprises reacting a halomethyl thiazole having the formula: with water, at an elevated temperature. Optionally, the reaction can be carried out in the presence of a base, such as sodium carbonate, which can react with any acid formed. In the process of the invention, X is a halogen atom; and R6 is selected from the group consisting of hydrogen, and halogen atoms. The invention also contemplates the preparation of acid addition salts of the hydroxymethylthiazole, compound 3.

公开(公告)号：AT251616T

公开(公告)日：2003-10-15

申请号：AT98942099

申请日：1998-08-18

Applicant: ABBOTT LAB

Inventor： ALLEN MICHAEL S

IPC: C07D277/20 ,  C07D277/22 ,  C07D277/24 ,  C07D277/32

Abstract: The present invention discloses a process for the preparation of a hydroxymethylthiazole compound having formula 3: The process of the invention comprises reacting a halomethyl thiazole having the formula: with water, at an elevated temperature. Optionally, the reaction can be carried out in the presence of a base, such as sodium carbonate, which can react with any acid formed. In the process of the invention, X is a halogen atom; and R6 is selected from the group consisting of hydrogen, and halogen atoms. The invention also contemplates the preparation of acid addition salts of the hydroxymethylthiazole, compound 3.

公开(公告)号：DK0916646T3

公开(公告)日：2003-08-25

申请号：DK99101692

申请日：1994-09-26

Applicant: ABBOTT LAB

Inventor： KERDESKY FRANCIS A J ,  NORBECK DANIEL W ,  ALLEN MICHAEL S ,  LANGRIDGE DENTON C ,  MELCHER LAURA ,  RENO DANIEL S ,  SHAM HING LEUNG ,  LEANNA M ROBERT ,  MORTON HOWARD E ,  ROBBINS TIMOTHY A ,  STUK TIMOTHY L ,  LIJEWSKI-LINCH LINDA M ,  SCARPETTI DAVID ,  TIEN JIEN-HEH J ,  ZHAO CHEN ,  HAIGHT ANTHONY R ,  SOWIN THOMAS J

IPC: C07C213/00 ,  C07C215/28 ,  C07C225/16 ,  C07C227/18 ,  C07C229/36 ,  C07C231/12 ,  C07C233/35 ,  C07C251/40 ,  C07C255/27 ,  C07C255/42 ,  C07C269/06 ,  C07C271/20 ,  C07D209/44 ,  C07D221/14

Abstract: Processes are disclosed which are useful for the preparation of a substantially pure compound of formula (3), wherein R6 and R7 are each hydrogen or R6 and R7 are independently selected from (i), wherein Ra and Rb are independently selected from hydrogen, loweralkyl and phenyl and Rc, Rd and Re are independently selected from hydrogen, loweralkyl, trifluoromethyl, alkoxy, halo and phenyl; and (ii) wherein the naphthyl ring is unsubstituted or substituted with one, two or three substituents independently selected from loweralkyl, trifluoromethyl, alkoxy, and halo; or R6 is as defined above and R7 is R7aOC (O)- wherein R7a is loweralkyl or benzyl; or R6 and R7 taken together with the nitrogen atom to which they are bonded are (a) or (b), wherein Rf, Rg, Rh and Ri are independently selected from hydrogen, loweralkyl, alkoxy, halogen, and trifluoromethyl and R8 is hydrogen or -C(O)R'' wherein R'' is loweralkyl, alkoxy, benzyloxy or phenyl wherein the phenyl ring is unsubstituted or substituted with one, two or three substituents independently selected from loweralkyl, trifluoromethyl, alkoxy and halo; or an acid addition salt thereof.

公开(公告)号：CY1113070T1

公开(公告)日：2016-04-13

申请号：CY121100626

申请日：2012-07-13

Applicant: ABBOTT LAB

Inventor： ALLEN MICHAEL S ,  PREMCHANDRAN RAMIYA H ,  CHANG SOU-JEN ,  CONDON STEPHEN ,  DEMATTEI JOHN J ,  KING STEVEN A ,  KOLACZKOWSKI LAWRENCE ,  MANNA SUKUMAR ,  NICHOLS PAUL J ,  PATEL HEMANT H ,  PATEL SUBHASH R ,  PLATA DANIEL J ,  STONER ERIC J ,  TIEN JIEN-HEH J ,  WITTENBERGER STEVEN J

IPC: C07D215/14 ,  C07C33/03 ,  C07C43/303 ,  C07C47/22 ,  C07C57/04 ,  C07C68/06 ,  C07C69/96 ,  C07C269/06 ,  C07C271/12 ,  C07D215/18 ,  C07D401/12 ,  C07H17/08

Abstract: Ηεφεύρεσηαφοράσεμιαμέθοδογιαπαρασκευήκινολινο-υποκατεστημένωνενώσεωνανθρακικούκαικαρβαμικού, οιοποίεςείναισημαντικάενδιάμεσαστηνσύνθεσητωναντιβιοτικών 6-O-υποκατεστημένουμακρολιδίου. Ημέθοδοςχρησιμοποιείτιςκαταλυόμενεςαπόμέταλλοαντιδράσειςσύζευξηςγιαναπαρέχειανθρακικόή καρβαμικότουτύπου (Ι) ή (II) ήυπόστρωμαπουμπορείναανάγεταιγιαναληφθούναυτά.

公开(公告)号：CA2368768C

公开(公告)日：2011-10-11

申请号：CA2368768

申请日：2000-06-15

Applicant: ABBOTT LAB

Inventor： ALLEN MICHAEL S ,  PREMCHANDRAN RAMIYA H ,  CHANG SOU-JEN ,  CONDON STEPHEN ,  DEMATTEI JOHN J ,  KING STEVEN A ,  KOLACZKOWSKI LAWRENCE ,  MANNA SUKUMAR ,  NICHOLS PAUL J ,  PATEL HEMANT H ,  PATEL SUBHASH R ,  PLATA DANIEL J ,  STONER ERIC J ,  TIEN JIEN-HEH J ,  WITTENBERGER STEVEN J

IPC: C07D215/14 ,  C07C68/06 ,  C07D215/18 ,  C07D401/12 ,  C07H17/08

Abstract: The invention relates to a process for preparing quinoline-substituted carbonate and carbamate compounds, which are important intermediates in the synthesis of 6-O-substituted macrolide antibiotics. The process employs metal-catalyzed coupling reactions to provide a carbonate or carbamate of formula (I) or (II) or a substrate that can be reduced to obtain the same.

公开(公告)号：CA2719425A1

公开(公告)日：2001-01-04

申请号：CA2719425

申请日：2000-06-15

Applicant: ABBOTT LAB

Inventor： ALLEN MICHAEL S ,  PREMCHANDRAN RAMIYA H ,  CHANG SOU-JEN ,  CONDON STEPHEN ,  DEMATTEI JOHN J ,  KING STEVEN A ,  KOLACZKOWSKI LAWRENCE ,  MANNA SUKUMAR ,  NICHOLS PAUL J ,  PATEL HEMANT H ,  PATEL SUBHASH R ,  PLATA DANIEL J ,  STONER ERIC J ,  TIEN JIEN-HEH J ,  WITTENBERGER STEVEN J

IPC: C07D215/14 ,  C07C33/03 ,  C07C43/303 ,  C07C47/22 ,  C07C57/04 ,  C07C68/06 ,  C07C69/54 ,  C07C69/96 ,  C07C271/08 ,  C07D215/12 ,  C07D215/18 ,  C07D401/12 ,  C07H17/08

Abstract: The invention relates to a process for preparing quinoline-substituted carbonate and carbamate compounds, which are important intermediates in the synthesis of 6-O-substituted marcolide antibiotics. The process employs metal-catalyzed coupling reactions to provide a carbonate or carbamate of formula (I) or (II) or substrate that can be reduced to obtain the same.

公开(公告)号：CA2368768A1

公开(公告)日：2001-01-04

申请号：CA2368768

申请日：2000-06-15

Applicant: ABBOTT LAB

Inventor： CONDON STEPHEN ,  CHANG SOU-JEN ,  DEMATTEI JOHN J ,  WITTENBERGER STEVEN J ,  PATEL HEMANT H ,  KING STEVEN A ,  PATEL SUBHASH R ,  MANNA SUKUMAR ,  NICHOLS PAUL J ,  STONER ERIC J ,  TIEN JIEN-HEH J ,  ALLEN MICHAEL S ,  KOLACZKOWSKI LAWRENCE ,  PLATA DANIEL J ,  PREMCHANDRAN RAMIYA H

IPC: C07C68/06 ,  C07D215/14 ,  C07D215/18 ,  C07D401/12 ,  C07H17/08 ,  C07C33/03 ,  C07C57/04 ,  C07C269/06 ,  C07C271/12 ,  C07C47/22 ,  C07C43/303 ,  C07C69/96

Abstract: The invention relates to a process for preparing quinoline-substituted carbonate and carbamate compounds, which are important intermediates in the synthesis of 6-O-substituted macrolide antibiotics. The process employs meta l- catalyzed coupling reactions to provide a carbonate or carbamate of formula (I) or (II) or a substrate that can be reduced to obtain the same.

公开(公告)号：CA2294089A1

公开(公告)日：1999-03-11

申请号：CA2294089

申请日：1998-08-18

Applicant: ABBOTT LAB

Inventor： ALLEN MICHAEL S

IPC: C07D277/20 ,  C07D277/22 ,  C07D277/24 ,  C07D277/32

Abstract: The present invention discloses a process for the preparation of a hydroxymethylthiazole compound having formula (3). The process of the invention comprises reacting a halomethyl thiazole having formula (A) with water, at an elevated temperature. Optionally, the reaction can be carried out in the presence of a base, such as sodium carbonate, which can react with any acid formed. In the process of the invention, X is a halogen atom; and R6 is selected from the group consisting of hydrogen, and halogen atoms. The invention also contemplates the preparation of acid addition salts of the hydroxymethylthiazole, compound (3).