2(1H)-Pyridinone, 5-iodo-1-methyl- → HCID 86607254, compound

HRID 502103Notes

Reaction equation

HRID 502103 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.I[C:30]1[CH:31]=[CH:32][C:33](=[O:37])[N:34]([CH3:36])[CH:35]=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:30]2[CH:31]=[CH:32][C:33](=[O:37])[N:34]([CH3:36])[CH:35]=2)=[CH:25][CH:26]=1

Participants

3

Reactant 2

HCID 234243102(1H)-Pyridinone, 5-iodo-1-methyl-HCID 866006811-Chloro-2-(4-ethynyl-benzyl)-4-(beta-D-glucopyranos-1-yl)-benzene

Product 1

HCID 86607254HCID 86607254, compound

Procedure

The compound was obtained starting from 1-chloro-4-(β-D-glucopyranos-1-yl)-2-(4-ethynyl-benzyl)-benzene and 5-iodo-1-methyl-1H-pyridin-2-one.

Workup

  1. customThe compound was obtained

Sources & evidence

ORD record
ord-9ca37739919c405cab4353f69694745b
Source dataset
uspto-grants-2010_08
Patent number
US07772378B2

Reaction notes

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