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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485693Generated: October 30, 2026

Isopropyl chloroformate → HCID 118079263, compound

https://huagongshe.com/reaction/1485693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl chloroformateHCID 7917—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-1-(6-bromo-2-methyl-3,4-dihydroquinoxalin-1(2H)-yl)ethanoneHCID 118078861—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 118079263HCID 11807926385%

Reaction Conditions

Temperature50 °C

Reaction Steps

N,N-Diisopropylethylamine (0.973 mL, 5.57 mmol) was added to a solution of (S)-1-(6-bromo-2-methyl-3,4-dihydroquinoxaline-1(2H)-yl)ethanone (0.500 g, 1.858 mmol) and isopropyl chloroformate (1.0 M in toluene, 2.79 mL, 2.79 mmol) in 1,2-dichloroethane (10.0 mL), and the mixture stirred at 50° C. for 16 h. The reaction mixture was concentrated to afford a yellow oil. This material was purified via column chromatography on silica gel (Biotage 25 g column, gradient elution with 0-50% ethyl acetate-hexane) to afford (S)-isopropyl 4-acetyl-7-bromo-3-methyl-3,4-dihydroquinoxaline-1(2H)-carboxylate (0.558 g, 85%) as an off-white solid. MS (ESI, pos. ion) m/z 355, 357 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422281B2
Source datasetuspto-grants-2016_08
ORD IDord-8fade10191514e06a86459ab733bfda6
Source noteuspto-grants-2016_08