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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486753Generated: October 29, 2026

HCID 18965166, compound → HCID 54561088, compound

https://huagongshe.com/reaction/486753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18965166HCID 18965166—
ReactantHCID 86747645HCID 86747645—
SolventAcetic AcidHCID 176—
SolventHydrogen BromideHCID 260—
ProductHCID 54561088HCID 54561088—

Reaction Conditions

Temperature25 °C

Reaction Steps

A 2.13 g (3 96 mmole) portion of (S)-4-(benzyloxycarbonyl)-1-[N-(3-bromophenyl-N-phenylcarbamoyl]piperazine-2-carboxylic acid (from Step B) was dissolved in 40 ml of 30% HBr in acetic acid. After stirring for 1 hour at 25° C., the solution was flushed with nitrogen to remove the excess of HBr. Concentration in vacuo gave an oily residue which was partitioned between 100 ml of methylene chloride and 100 ml of water. The stirred slurry was neutralized to pH 7 with 10% NaOH solution. After a brief stirring the entire mixture was filtered to collect 1.50 g (3.71 mmole, 94%) of white solid which was homogeneous by TLC (5:1:1:1 ethyl acetate-n-butyl alcohol-ethyl acetate-water Rf =0.33).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292726
Source datasetuspto-grants-1994_03
ORD IDord-ae080796a13d45f7880b704717902b8c
Source noteuspto-grants-1994_03