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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979380Generated: November 4, 2026

Chloride → HCID 21201649, compound

https://huagongshe.com/reaction/1979380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantEthyl 3-aminobenzoateHCID 11400—
ReactantTriphosgeneHCID 94429—
ReactantHCID 21201731HCID 21201731—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 21201649HCID 21201649223.5%

Reaction Steps

Ethyl 3-aminobenzoate (69 mg) was dissolved in tetrahydrofuran (10 ml), the solution was cooled on ice-water. Triphosgene (45 mg) was added at internal temperature 5° C., triethylamine (162 mg) was added thereto over 10 minutes period, the mixture was allowed to come to room temperature and stirred for 10 minutes. A solution of 1-tert-butylcarbonylmethyl-2-oxo-3-amino-5-(2-fluorophenyl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (150 mg) in tetrahydrofuran (5 ml), the mixture was additionally chloride. The organic layer was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography(n-hexane:ethyl acetate=3:1), to thereby obtain 190 mg of the title compound as colorless crystals (Yield: 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239131B1
Source datasetuspto-grants-2001_05
ORD IDord-d58a158b89b14b26afd1e6ec05a8f33c
Source noteuspto-grants-2001_05