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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034088Generated: October 31, 2026

Hydrochloric Acid → benzyl 4-[3-[3-(N-benzyl-N-tert-butoxycarbonylamino)benzoyl]indol-1-yl]butyrate

https://huagongshe.com/reaction/1034088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant4-[3-(3-Tert-butoxycarbonylaminobenzoyl)indol-1-yl]butyric acidHCID 19024725—
SolventDimethylformamideHCID 6228—
Productbenzyl 4-[3-[3-(N-benzyl-N-tert-butoxycarbonylamino)benzoyl]indol-1-yl]butyrateHCID 1902483196.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

60% Sodium hydride in mineral oil (0.13 g) was added to a solution of 4-[3-(3-tert-butoxycarbonylaminobenzoyl)-indol-1-yl]butyric acid (0.47 g) in N,N-dimethylformamide (7 ml). The mixture was stirred at 0° C. for 1 hour. Benzyl bromide (0.95 g) was added to the mixture and the mixture was stirred at room temperature for 20 hours. The mixture was poured into ice water and 0.5N-hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (30 g) eluting with a mixture of n-hexane and ethyl acetate (5:1) to give benzyl 4-[3-[3-(N-benzyl-N-tert-butoxycarbonylamino)benzoyl]indol-1-yl]butyrate (325 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312829
Source datasetuspto-grants-1994_05
ORD IDord-27f882def41e411fa821859c8bce3a91
Source noteuspto-grants-1994_05