HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485742Generated: November 1, 2026
Cyclopropanecarbonyl chloride → HCID 118079498, compound
https://huagongshe.com/reaction/1485742
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 118080245 | HCID 118080245 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 118079498 | HCID 118079498 | 100.2% |
Reaction Steps
N,N-Diisopropylethylamine (0.041 mL, 0.232 mmol) was added to a solution of (S)-2-(7-bromo-3-methyl-3,4-dihydroquinoxaline-1(2H)-yl)benzo[d]oxazole (0.016 g, 0.046 mmol) and cyclopropanecarbonyl chloride (0.021 mL, 0.232 mmol) in 1,2-dichloroethane (1.0 mL), and the mixture stirred at 50° C. for 2.5 h. The reaction mixture was partitioned between water and dichloromethane. The aqueous phase was separated and extracted with dichloromethane. The combined organic phases were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford (S)-(4-(benzo[d]oxazol-2-yl)-6-bromo-2-methyl-3,4-dihydroquinoxaline-1(2H)-yl)(cyclopropyl)methanone (0.019 g, 99%) as a brown oil. MS (ESI, pos. ion) m/z 412, 414 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422281B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-64407ede47e24d06b4bf936d7eb98ee7 |
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| Source note | uspto-grants-2016_08 |
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