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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415250Generated: October 29, 2026

Azane;hydrate → Benzyl 2-(7-carbamoylbenzo[d]oxazol-2-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/415250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzane;hydrateHCID 12896473—
ReactantMethyl 2-(1-(benzyloxycarbonyl)pyrrolidin-2-yl)benzo[d]oxazole-7-carboxylateHCID 66621250—
SolventMethanolHCID 887—
ProductBenzyl 2-(7-carbamoylbenzo[d]oxazol-2-yl)pyrrolidine-1-carboxylateHCID 6662118842%

Reaction Steps

To a stirred solution of methyl 2-(1-(benzyloxycarbonyl)pyrrolidin-2-yl)benzo[d]oxazole-7-carboxylate (150 mg, 0.394 mmol) in methanol (8 mL) was added ammonia water (6 mL) at 0° C. After the addition, the mixture was allowed to stir at room temperature overnight. Methanol was removed in vacuum. The residue was diluted with water (100 mL), extracted with ethyl acetate (50 mL×3). The combined organic layers washed with brine, dried over anhydrous sodium sulfate, and concentrated to give crude product. The crude product was purified by chromatography (silica gel, petroleum ether/ethyl acetate=20:1 to 1:1) to give benzyl 2-(7-carbamoylbenzo[d]oxazol-2-yl)pyrrolidine-1-carboxylate (68 mg, yield 42%). LC-MS (ESI) m/z: 366 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-0c7138c79e374084b98397d109a18bb9
Source noteuspto-grants-2012_01