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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289257Generated: November 2, 2026

HCID 178451023, compound → HCID 178451024, compound

https://huagongshe.com/reaction/1289257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178451023HCID 178451023—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 178451024HCID 178451024—

Reaction Steps

A solution of tert-butyl (4R)-4-{N-[N-(benzyloxycarbonyl)-αtert-butyl-(S)-γ-glutamyl]amino}-4-(tetrazol-5-yl)butyrate (0.320 g, 0.585 mmol) in ethanol (35 ml) was stirred with 10% Pd-C. (0.12 g) under a hydrogen atmosphere at ambient temperature. After 16 hours further 10% Pd-C. (0.09 g) was added and the mixture was stirred under hydrogen for a further 6 hours. It was then filtered through Celite and the filtrate was evaporated. Several portions of dichloromethane were added and evaporated to leave tert-butyl (4R)-4-[N-(α-tert-butyl-(S)-γ-glutamyl)amino]-4-(tetrazol-5-yl)butyrate as a crisp, colourless glass which was dried over phosphorus pentoxide and used without further purification. Yield 0.24 g; m.p. 92°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747499
Source datasetuspto-grants-1998_05
ORD IDord-143e9a10dba040e482c45ccd8a811331
Source noteuspto-grants-1998_05