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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485725Generated: November 1, 2026

Cyclopropanecarbonyl chloride → HCID 118078957, compound

https://huagongshe.com/reaction/1485725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 118079994HCID 118079994—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 118078957HCID 11807895798%

Reaction Conditions

Temperature50 °C

Reaction Steps

N,N-Diisopropylethylamine (0.486 mL, 2.79 mmol) was added to a solution of (S)-1-(6-bromo-2-methyl-3,4-dihydroquinoxaline-1(2H)-yl)-2,2,2-trifluoroethanone (0.300 g, 0.928 mmol) and cyclopropanecarbonyl chloride (0.126 mL, 1.39 mmol) in 1,2-dichloroethane (6.0 mL), and the mixture stirred at 50° C. for 16 h. The reaction mixture was concentrated to afford an orange oil. This material was purified via column chromatography on silica gel (Biotage 25 g column, gradient elution with 0-25% ethyl acetate-hexane) to afford (S)-1-(6-bromo-4-(cyclopropanecarbonyl)-2-methyl-3,4-dihydroquinoxaline-1(2H)-yl)-2,2,2-trifluoroethanone (0.355 g, 98%) as a yellow oil. MS (ESI, pos. ion) m/z 435, 437 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422281B2
Source datasetuspto-grants-2016_08
ORD IDord-5dd1bc30b29d447aa191a6b5e1d2e747
Source noteuspto-grants-2016_08