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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784240Generated: November 1, 2026

Hydrochloric Acid → (S)-2-(5-Amino-2-chloro-benzoylamino)-3-(4-bromo-phenyl)-propionic acid methyl ester

https://huagongshe.com/reaction/1784240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Amino-2-chlorobenzoic acidHCID 37879—
Reactant(S)-Methyl 2-amino-3-(4-bromophenyl)propanoate hydrochlorideHCID 24720902—
SolventEthyl AcetateHCID 8857—
Product(S)-2-(5-Amino-2-chloro-benzoylamino)-3-(4-bromo-phenyl)-propionic acid methyl esterHCID 6886154815.1%

Reaction Steps

(S)-2-(5-Amino-2-chloro-benzoylamino)-3-(4-bromo-phenyl)-propionic acid methyl ester (316 mg) was prepared from (S)-2-Amino-3-(4-bromo-phenyl)-propionic acid methyl ester-hydrochloride (1.5 g, 5.1 mmol) and 5-amino-2-chloro-benzoic acid (909 mg, 5.1 mmol) as described in Procedure A, except for an adapted work-up. After reaction completion, the reaction mixture was poured onto 100 mL of 1N HCl and 50 mL of EtOAc. The organic layer was washed with 1N HCl, 10% sodium carbonate, dried over sodium sulfate and evaporated. The crude material was purified over silica gel (DCM-EtOAc, 9-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501538B2
Source datasetuspto-grants-2009_03
ORD IDord-95f10ea146fa4dd798c4b19d25e814d7
Source noteuspto-grants-2009_03