HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743879Generated: October 30, 2026
1-Chloroethyl chloroformate → HCID 10244387, compound
https://huagongshe.com/reaction/1743879
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 10446058 | HCID 10446058 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 10244387 | HCID 10244387 | 73.7% |
Reaction Steps
To a solution of 8-chloro-3-methyl-2,3,4,5,10,11-hexahydro-1H,9H-cyclopenta[b][1,4]diazocino[7,8,1-hi]indole (1.0 g, 3.64 mmole) in dichloroethane (200 mL) was added 1-chloroethyl chloroformate (2.0 mL, 18.35 mmole) and refluxed for 24 hours. The reaction mixture was cooled to room temperature and the solvent removed in vacuo and replaced with methanol (200 mL) and refluxed for another 3 hours. The reaction mixture was cooled to room temperature and the solvent removed in vacuo. The dark residue was dissolved in methylene chloride (200 mL) and washed with aqueous sodium hydroxide (1N, 150 mL), saturated sodium chloride (150 mL), dried (sodium sulfate) and concentrated. Purification by flash column chromatography (silica gel, 1.5% to 3% methanol in dichloromethane) provided 0.70 g of the title compound as a white solid. 0.12 g of the above solid was further treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 226-228° C. MS (ES) m/z 261.09 ([M+H]+), MS (ES) m/z 302.12 ([M+ACN+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07012089B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-dd5d7cdca86646b4967188703032fab8 |
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| Source note | uspto-grants-2006_03 |
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