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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829097Generated: November 2, 2026

Water → methyl (2S,4R)-4-(2-benzoxazolyl)amino-1-tert-butoxycarbonylpyrrolidine-2-carboxylate

https://huagongshe.com/reaction/1829097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactant1-tert-butyl 2-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylateHCID 7009918—
SolventTetrahydrofuranHCID 8028—
Productmethyl (2S,4R)-4-(2-benzoxazolyl)amino-1-tert-butoxycarbonylpyrrolidine-2-carboxylateHCID 69754879—

Reaction Steps

Methyl (2S,4R)-4-amino-1-tert-butoxycarbonylpyrrolidine-2-carboxylate [product of Reference Example 4(2), 3.32 g] and triethylamine (1.4 mL) were dissolved in tetrahydrofuran (20 mL). 2-Chlorobenzoxazole (0.86 mL) was added thereto and the mixture was stirred at room temperature for 48 hr. The reaction mixture was added to water and extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogencarbonate solution and brine, and dried. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography to give methyl (2S,4R)-4-(2-benzoxazolyl)amino-1-tert-butoxycarbonylpyrrolidine-2-carboxylate (1.48 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060722B2
Source datasetuspto-grants-2006_06
ORD IDord-eaa19e6c702945bb9f7355d9aeba09dd
Source noteuspto-grants-2006_06