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Development of a manufacturing route to 1-hydroxy-4-(3-pyridyl)butan-2-one using heck methodology
被引:6
作者
:
Ainge, D
论文数:
0
引用数:
0
h-index:
0
机构:
AstraZeneca, Proc Res & Dev Dept, Loughborough LE11 5RH, Leics, England
AstraZeneca, Proc Res & Dev Dept, Loughborough LE11 5RH, Leics, England
Ainge, D
[
1
]
Vaz, LM
论文数:
0
引用数:
0
h-index:
0
机构:
AstraZeneca, Proc Res & Dev Dept, Loughborough LE11 5RH, Leics, England
AstraZeneca, Proc Res & Dev Dept, Loughborough LE11 5RH, Leics, England
Vaz, LM
[
1
]
机构
:
[1]
AstraZeneca, Proc Res & Dev Dept, Loughborough LE11 5RH, Leics, England
来源
:
ORGANIC PROCESS RESEARCH & DEVELOPMENT
|
2002年
/ 6卷
/ 06期
关键词
:
D O I
:
10.1021/op0255736
中图分类号
:
O69 [应用化学];
学科分类号
:
081704 ;
摘要
:
The optimisation and scale-up of a manufacturing route to a key intermediate, 1-hydroxy-4-(3-pyridyl)butan-2-one, utilising the Heck coupling of 3-bromopyridine and 3-butene-1,2-diol, is described.
引用
收藏
页码:811 / 813
页数:3
相关论文
共 9 条
[1]
CHESHIRE D, Patent No. 9720815
[2]
HUBSCHWERLEN C, 1986, SYNTHESIS-STUTTGART, P962
[3]
HECK-TYPE REACTIONS IN WATER
JEFFERY, T
论文数:
0
引用数:
0
h-index:
0
机构:
Laboratoire de Chimie, l'Ecole Normale Supérieure associé au CNRS -, 75231 Paris Cédex 05, 24, Rue Lhomond
JEFFERY, T
[J].
TETRAHEDRON LETTERS,
1994,
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: 3051
-
3054
[4]
EFFICIENT PROCEDURES FOR INSITU TRAPPING OF (R)-GLYCERALDEHYDE AND (S)-GLYCERALDEHYDE ACETONIDES BY STABILIZED WITTIG REAGENTS
LEONARD, J
论文数:
0
引用数:
0
h-index:
0
LEONARD, J
MOHIALDIN, S
论文数:
0
引用数:
0
h-index:
0
MOHIALDIN, S
SWAIN, PA
论文数:
0
引用数:
0
h-index:
0
SWAIN, PA
[J].
SYNTHETIC COMMUNICATIONS,
1989,
19
(20)
: 3529
-
3534
[5]
Heck reactions in the presence of p(t-bu)3:: Expanded scope and milder reaction conditions for the coupling of aryl chlorides
Littke, AF
论文数:
0
引用数:
0
h-index:
0
机构:
MIT, Dept Chem, Cambridge, MA 02139 USA
MIT, Dept Chem, Cambridge, MA 02139 USA
Littke, AF
Fu, GC
论文数:
0
引用数:
0
h-index:
0
机构:
MIT, Dept Chem, Cambridge, MA 02139 USA
MIT, Dept Chem, Cambridge, MA 02139 USA
Fu, GC
[J].
JOURNAL OF ORGANIC CHEMISTRY,
1999,
64
(01)
: 10
-
11
[6]
A reliable multikilogram-scale synthesis of 2-acetamido-5-vinylpyridine using catalytic BINAP in a modified Heck reaction
Raggon, JW
论文数:
0
引用数:
0
h-index:
0
机构:
Pfizer Inc, Pharmaceut Sci Div, Chem Res & Dev Dept, Groton, CT 06240 USA
Pfizer Inc, Pharmaceut Sci Div, Chem Res & Dev Dept, Groton, CT 06240 USA
Raggon, JW
Snyder, WM
论文数:
0
引用数:
0
h-index:
0
机构:
Pfizer Inc, Pharmaceut Sci Div, Chem Res & Dev Dept, Groton, CT 06240 USA
Pfizer Inc, Pharmaceut Sci Div, Chem Res & Dev Dept, Groton, CT 06240 USA
Snyder, WM
[J].
ORGANIC PROCESS RESEARCH & DEVELOPMENT,
2002,
6
(01)
: 67
-
69
[7]
Reetz MT, 1998, ANGEW CHEM INT EDIT, V37, P481, DOI 10.1002/(SICI)1521-3773(19980302)37:4<481::AID-ANIE481>3.0.CO
[8]
2-I
[9]
A highly active phosphine-free catalyst system for Heck reactions of aryl bromides
Reetz, MT
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Reetz, MT
Westermann, E
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Westermann, E
Lohmer, R
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Lohmer, R
Lohmer, G
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Lohmer, G
[J].
TETRAHEDRON LETTERS,
1998,
39
(46)
: 8449
-
8452
←
1
→
共 9 条
[1]
CHESHIRE D, Patent No. 9720815
[2]
HUBSCHWERLEN C, 1986, SYNTHESIS-STUTTGART, P962
[3]
HECK-TYPE REACTIONS IN WATER
JEFFERY, T
论文数:
0
引用数:
0
h-index:
0
机构:
Laboratoire de Chimie, l'Ecole Normale Supérieure associé au CNRS -, 75231 Paris Cédex 05, 24, Rue Lhomond
JEFFERY, T
[J].
TETRAHEDRON LETTERS,
1994,
35
(19)
: 3051
-
3054
[4]
EFFICIENT PROCEDURES FOR INSITU TRAPPING OF (R)-GLYCERALDEHYDE AND (S)-GLYCERALDEHYDE ACETONIDES BY STABILIZED WITTIG REAGENTS
LEONARD, J
论文数:
0
引用数:
0
h-index:
0
LEONARD, J
MOHIALDIN, S
论文数:
0
引用数:
0
h-index:
0
MOHIALDIN, S
SWAIN, PA
论文数:
0
引用数:
0
h-index:
0
SWAIN, PA
[J].
SYNTHETIC COMMUNICATIONS,
1989,
19
(20)
: 3529
-
3534
[5]
Heck reactions in the presence of p(t-bu)3:: Expanded scope and milder reaction conditions for the coupling of aryl chlorides
Littke, AF
论文数:
0
引用数:
0
h-index:
0
机构:
MIT, Dept Chem, Cambridge, MA 02139 USA
MIT, Dept Chem, Cambridge, MA 02139 USA
Littke, AF
Fu, GC
论文数:
0
引用数:
0
h-index:
0
机构:
MIT, Dept Chem, Cambridge, MA 02139 USA
MIT, Dept Chem, Cambridge, MA 02139 USA
Fu, GC
[J].
JOURNAL OF ORGANIC CHEMISTRY,
1999,
64
(01)
: 10
-
11
[6]
A reliable multikilogram-scale synthesis of 2-acetamido-5-vinylpyridine using catalytic BINAP in a modified Heck reaction
Raggon, JW
论文数:
0
引用数:
0
h-index:
0
机构:
Pfizer Inc, Pharmaceut Sci Div, Chem Res & Dev Dept, Groton, CT 06240 USA
Pfizer Inc, Pharmaceut Sci Div, Chem Res & Dev Dept, Groton, CT 06240 USA
Raggon, JW
Snyder, WM
论文数:
0
引用数:
0
h-index:
0
机构:
Pfizer Inc, Pharmaceut Sci Div, Chem Res & Dev Dept, Groton, CT 06240 USA
Pfizer Inc, Pharmaceut Sci Div, Chem Res & Dev Dept, Groton, CT 06240 USA
Snyder, WM
[J].
ORGANIC PROCESS RESEARCH & DEVELOPMENT,
2002,
6
(01)
: 67
-
69
[7]
Reetz MT, 1998, ANGEW CHEM INT EDIT, V37, P481, DOI 10.1002/(SICI)1521-3773(19980302)37:4<481::AID-ANIE481>3.0.CO
[8]
2-I
[9]
A highly active phosphine-free catalyst system for Heck reactions of aryl bromides
Reetz, MT
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Reetz, MT
Westermann, E
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Westermann, E
Lohmer, R
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Lohmer, R
Lohmer, G
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
Lohmer, G
[J].
TETRAHEDRON LETTERS,
1998,
39
(46)
: 8449
-
8452
←
1
→