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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034083Generated: October 25, 2026

Hydrochloric Acid → HCID 19024829, compound

https://huagongshe.com/reaction/1034083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant1-(Chloromethyl)-4-(2-methylpropyl)benzeneHCID 181289—
ReactantHCID 19024802HCID 19024802—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 19024829HCID 19024829170.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethyl 4-[3-[3,5-bis(tertbutoxycarbonylamino)benzoyl]indol-1-yl]butyrate (300 mg) in N,N-dimethylformamide (5 ml) was added to a suspension of sodium hydride (60% dispersion in mineral oil, 54 mg) in N,N-dimethylformamide (5 ml ) at 0° C. The mixture was stirred at 0° C. for 30 minutes, and a solution of 4-isobutylbenzyl chloride (38.8 mg) in N,N-dimethylformamide (5 ml) was added at 0° C. The reaction mixture was stirred at 0° C. for 3 hours, and poured into a mixture of 0.1N hydrochloric acid and ethyl acetate. The organic layer was separated, washed with water, aqueous solution of sodium bicarbonate and brine in successively. After dryness over magnesium sulfate and evaporation of the solvent, the residue was chromatographed on silica gel (25 g) eluting with a mixture of ethyl acetate and hexane (1:4) to give ethyl 4-[3-[3,5-bis[N-(4-isobutylbenzyl )-N-tert-butoxycarbonylamino] benzoyl]indol-1-yl]butyrate (155 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312829
Source datasetuspto-grants-1994_05
ORD IDord-9f2f8998782a46b59aae0344684c6ff5
Source noteuspto-grants-1994_05