5-Bromo-2-methoxypyridine → 1-Chloro-4-(beta-D-glucopyranos-1-yl)-2-[4-(2-methoxy-pyridin-5-yl-ethynyl)-benzyl]-benzene
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@:8]2([O:17][C@H:16]([CH2:18][OH:19])[C@@H:14]([OH:15])[C@H:12]([OH:13])[C@H:10]2[OH:11])[OH:9])=[CH:4][C:3]=1[CH2:20][C:21]1[CH:26]=[CH:25][C:24]([C:27]#[CH:28])=[CH:23][CH:22]=1.[CH3:29][O:30][C:31]1[CH:36]=[CH:35][C:34](Br)=[CH:33][N:32]=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@:8]2([O:17][C@H:16]([CH2:18][OH:19])[C@@H:14]([OH:15])[C@H:12]([OH:13])[C@H:10]2[OH:11])[OH:9])=[CH:4][C:3]=1[CH2:20][C:21]1[CH:22]=[CH:23][C:24]([C:27]#[C:28][C:34]2[CH:35]=[CH:36][C:31]([O:30][CH3:29])=[N:32][CH:33]=2)=[CH:25][CH:26]=1Participants
3
Procedure
The compound was obtained starting from 1-chloro-4-(β-D-glucopyranos-1-yl)-2-(4-ethynyl-benzyl)-benzene and 2-methoxy-5-bromo-pyridine.
Workup
- customThe compound was obtained
Sources & evidence
- ORD record
- ord-eb3a9205e12e45ee89105022f1615e97
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07772378B2
Reaction notes
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