Methoxyacetic Acid → HCID 59543567, compound

HRID 1697503Notes

Reaction equation

Cl.[C:2]([CH2:4][NH:5][C:6]([C@@H:8]1[CH2:12][C@@H:11]([S:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[Cl:22])(=[O:15])=[O:14])[CH2:10][NH:9]1)=[O:7])#[N:3].[CH3:23][O:24][CH2:25][C:26](O)=[O:27]>>[C:2]([CH2:4][NH:5][C:6]([C@@H:8]1[CH2:12][C@@H:11]([S:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[Cl:22])(=[O:14])=[O:15])[CH2:10][N:9]1[C:26](=[O:27])[CH2:25][O:24][CH3:23])=[O:7])#[N:3]

Participants

Reactant 2

HCID 12251Methoxyacetic Acid

HCID 86646813HCID 86646813, compound

Product 1

HCID 59543567HCID 59543567, compound

Procedure

L11. (2S,4R)-4-(2-chloro-benzenesulfonyl)-pyrrolidine-2-carboxylic acid cyanomethyl-amide hydrochloride from experiment K1 was coupled with methoxy-acetic acid in analogy to experiment A1 to give (2S,4R)-4-(2-chloro-benzenesulfonyl)-1-(2-methoxy-acetyl)-pyrrolidine-2-carboxylic acid cyanomethyl-amide as a colorless foam. MS: 400.1 [M+H]+.

Sources & evidence

ORD record: ord-67d856373306482cbfd511a76417f5cd
Source dataset: uspto-grants-2012_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08163793B2

Reaction notes

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