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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643828Generated: October 30, 2026

(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid → 4-[2-(2-Isopropylamino-thiazol-4-yl)-7-methoxy-quinolin-4-yloxy]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester

https://huagongshe.com/reaction/643828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acidHCID 88804—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178487686HCID 178487686—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-[2-(2-Isopropylamino-thiazol-4-yl)-7-methoxy-quinolin-4-yloxy]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl esterHCID 74955511—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of N-Boc-trans-4-hydroxy-L-proline (221 mg, 0.96 mmol) in DMSO was added potassium tert-butoxide (320 mg, 2.9 mmol). After 1 h compound 12 (319 mg, 0.96 mmol) was added and the mixture was stirred at 70° C. for 72 hours. The mixture was diluted with water and extracted with ethyl acetate. The product was used without further purification. Yield 429 mg, 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700552B2
Source datasetuspto-grants-2010_04
ORD IDord-b1d75f5cd2874471947e1f34efabce7d
Source noteuspto-grants-2010_04