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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737173Generated: October 30, 2026

(S)-2-[4-(4-Amino-phenyl)-thiazol-2-ylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl ester → 2-[4-(4-Ureido-phenyl)-thiazol-2-yl carbamoyl]-pyrrolidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/737173

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-[4-(4-Amino-phenyl)-thiazol-2-ylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl esterHCID 86616427—
Reactantdioxane TMS isocyanateHCID 86616432—
Product2-[4-(4-Ureido-phenyl)-thiazol-2-yl carbamoyl]-pyrrolidine-1-carboxylic acid benzyl esterHCID 59140923—

Reaction Conditions

Temperature70 °C

Reaction Steps

2-[4-(4-Amino-phenyl)-thiazol-2-ylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl ester (Compound 5050, Example 50, 40 mg, 0.095 mmol) was dissolved in 4 ml of 1:1 dioxane/TMS isocyanate. Reaction mixture was heated at 70° C. for 7 hours. It was then evaporated to dryness. The crude was redissolved in 10 ml of DMF and purified on reverse phase HPLC. MS: 466.1 (M+H+); H1 NMR (DMSO-d6): δ(ppm) 12.39 (d, 1H), 7.72 (d, 2H), 7.42 (d, 3H), 7.35 (s, 2H), 7.10 (dd, 2H), 5.88 (br s, 2H), 5.02 (m, 2H), 4.50 (m, 1H), 2.25 (m, 2H), 1.90 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595398B2
Source datasetuspto-grants-2009_09
ORD IDord-9bf98091e533456692eb761d3b5c0e78
Source noteuspto-grants-2009_09