HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793505Generated: November 3, 2026
Cyclopropanecarbonyl chloride → HCID 20576981, compound
https://huagongshe.com/reaction/1793505
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | HCID 20576996 | HCID 20576996 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20576981 | HCID 20576981 | — |
Reaction Steps
(±)-cis-4,5,6a,7,8,9,10,10a-octahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole from Example 3 (0.050 g, 0.25 mmol) was dissolved in CH2Cl2 (5 mL) with Et3N (0.75 mL) and cooled to 0° C. The cyclopropanecarbonyl chloride (0.026 g, 0.26 mmol) was then added dropwise. The solution was stirred at 0° C. for 1 h and then warmed to room temperature and stirred for 1 h. The reaction mixture was partitioned between water and CHCl3(3×15 mL) and the layers separated. The aqueous layer was extracted with CHCl3. The combined organics were washed with brine, H2O and dried (Na2SO4) and evaporated affording a light yellow liquid which was further purified by preparatory silica gel TLC (5% MeOH/CH2Cl2). The title compound was isolated as a clear colorless liquid (0.042 g, 65%). 1H NMR (CD3OD, 300 MHz) δ 7.22–7.58 (m, 3H), 4.62–4.75 (m, 1H), 3.85–4.30 (m, 5H), 3.55–3.62 (m, 2H), 1.9–2.18 (m, 3H), 0.75–0.9 (m, 4H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07081455B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-bcf0727f4d4244db8a03bf9cd2c4f315 |
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| Source note | uspto-grants-2006_07 |
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