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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466858Generated: October 25, 2026

Hydrogen Bromide → HCID 18648268, compound

https://huagongshe.com/reaction/466858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant3-[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-4(R)-thiazolidinecarboxamideHCID 57324410—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
ProductHCID 18648268HCID 18648268—

Reaction Steps

A mixture of 2 g of 3-[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-4(R)-thiazolidinecarboxamide and 4.1 ml of 32% (w/w) hydrogen bromide in glacial acetic acid was stirred at room temperature for 1 hour. The resulting solution was diluted with anhydrous diethyl ether and the precipitated product was rapidly filtered off and washed with fresh diethyl ether. There were obtained 2.01 g of 3-[3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-4(R)-thiazolidinecarboxamide dihydrobromide as a white solid; 1H NMR (300 MHz): δ (D2O) 1.37 (9H, s), 3.0 (2H, m), 3.09 (2H, dq), 3.29 (2H, d), 3.85 (2H, m), 4.16 (1H, m), 4.3 (2H, q) and 7.42 (5H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157041
Source datasetuspto-grants-1992_10
ORD IDord-c7291a3b69334947942eea4282d9d90f
Source noteuspto-grants-1992_10