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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270870Generated: October 31, 2026

Hydrochloric Acid → N-[2-chloro-4-[[(3-hydroxyphenyl) carbonyl]aminomethyl]benzoyl]-3-benzoylamino-L-alanine

https://huagongshe.com/reaction/2270870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Hydroxybenzoic AcidHCID 7420—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantN-[4-(aminomethyl)-2-chlorobenzoyl]-3-benzoylamino-L-alanine, methyl esterHCID 59977292—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductN-[2-chloro-4-[[(3-hydroxyphenyl) carbonyl]aminomethyl]benzoyl]-3-benzoylamino-L-alanineHCID 599772759.5%

Reaction Steps

A mixture of N-(aminomethyl)-2-chlorobenzoyl]-3-benzoylamino-L-alanine (Example 363; 100 mg, 0.26 mmol), 3-hydroxybenzoic acid (40 mg, 0.29 mmol) and dicyclohexylcarbodiimide (60 mg, 0.29 mmol) in tetrahydrofuran/DMF (4:1; 2.5 mL) was stirred at room temperature overnight. Methanol (1 mL) and a solution of lithium hydroxide monohydrate (100 mg, 2.4 mmol) in water (1 mL) were added and the solution was stirred at room temperature overnight. The solution was made acidic with 1 M HCl and extracted with ethyl acetate. The ethyl acetate was evaporated and the residue purified by HPLC to give N-[2-chloro-4-[[(3-hydroxyphenyl) carbonyl]aminomethyl]benzoyl]-3-benzoylamino-L-alanine (12.2 mg, 9%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331640B1
Source datasetuspto-grants-2001_12
ORD IDord-3a7ef3c2d55a413990a373621d78d3c1
Source noteuspto-grants-2001_12