HCID 59619202, compound → HCID 59619393, compound

HRID 1367558Notes

Reaction equation

HRID 1367558 reaction equation
[C:1]([C:3]1([NH:6][C:7]([C@@H:9]2[CH2:13][C@@H:12]([S:14]([C:17]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][C:18]=3[Cl:24])(=[O:16])=[O:15])[CH2:11][C@H:10]2[CH2:25][OH:26])=[O:8])[CH2:5][CH2:4]1)#[N:2].O[C:28]1[CH:33]=[CH:32][N:31]=[CH:30][CH:29]=1>>[C:1]([C:3]1([NH:6][C:7]([C@@H:9]2[CH2:13][C@@H:12]([S:14]([C:17]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][C:18]=3[Cl:24])(=[O:15])=[O:16])[CH2:11][C@H:10]2[CH2:25][O:26][C:28]2[CH:33]=[CH:32][N:31]=[CH:30][CH:29]=2)=[O:8])[CH2:5][CH2:4]1)#[N:2]

Participants

3

Reactant 2

HCID 59619202HCID 59619202, compoundHCID 178418642HCID 178418642, compound

Product 1

HCID 59619393HCID 59619393, compound

Procedure

The title compound was prepared in analogy to example 162 using (1R,2R,4S)-4-(2-chloro-4-fluoro-benzenesulfonyl)-2-hydroxymethyl-cyclopentanecarboxylic acid (1-cyano-cyclopropyl)-amide (example 155) and 4-hydroxypyridine. Colorless oil (22%). MS (EI): 478.1 (M+H)+.

Sources & evidence

ORD record
ord-2564607db8c545299a6560e567ddebc1
Source dataset
uspto-grants-2011_02
Patent number
US07893099B2

Reaction notes

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