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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025336Generated: November 2, 2026

(2S,4R)-1-(2-nitrophenyl)-4-(2-(trifluoromethyl)phenylsulfonyl)pyrrolidine-2-carboxylic acid → (2S,4R)-1-(2-Nitro-phenyl)-4-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidine-2-carboxylic acid [(S)-1-(benzooxazole-2-carbonyl)-propyl]-amide

https://huagongshe.com/reaction/1025336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,4R)-1-(2-nitrophenyl)-4-(2-(trifluoromethyl)phenylsulfonyl)pyrrolidine-2-carboxylic acidHCID 66770587—
Reactant(2S)-2-amino-1-(benzo[d]oxazol-2-yl)butan-1-ol dihydrochlorideHCID 86762432—
Product(2S,4R)-1-(2-Nitro-phenyl)-4-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidine-2-carboxylic acid [(S)-1-(benzooxazole-2-carbonyl)-propyl]-amideHCID 71577052—

Reaction Steps

The title compound was prepared in analogy to Example 1, using (2S,4R)-1-(2-nitrophenyl)-4-(2-(trifluoromethyl)phenylsulfonyl)pyrrolidine-2-carboxylic acid (prepared as described in U.S. Pat. Appl. US20100267722) and (2S)-2-amino-1-(benzo[d]oxazol-2-yl)butan-1-ol dihydrochloride in step 1. MS (m/e)=631.15 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729061B2
Source datasetuspto-grants-2014_05
ORD IDord-72a09f9d86dc460f81f926a20f1b6833
Source noteuspto-grants-2014_05