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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533285Generated: November 2, 2026

HCID 20640784, compound → HCID 178523863, compound

https://huagongshe.com/reaction/1533285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20640784HCID 20640784—
SolventWaterHCID 962—
SolventAcetic acid--water (1/1)HCID 21899381—
ProductHCID 178523863HCID 17852386390.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of Nα-[3-(1-triphenylmethylimidazol-4-yl)-2-(3,4-methylenedioxyphenyl)propionyl]-L-tryptophan benzyl ester (290 mg) in 80% acetic acid-water (5 ml) was stirred at 50° C. for 5 hours. The resulting mixture was cooled to ambient temperature and the solution was diluted with water. Carbinol was removed by filtration and the filtrate was neutralized with saturated sodium hydroxide aqueous solution, and then the aqueous layer was extracted with ethyl acetate. Drying, filtering and removal of the solvents afforded Nα-[3-(imidazol-4-yl)-2-(3,4-methylenedioxyphenyl)propionyl]-L-tryptophan benzyl ester (180 mg) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207686B1
Source datasetuspto-grants-2001_03
ORD IDord-81d422feea5b4aebb010a19bc49ebea6
Source noteuspto-grants-2001_03