HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743864Generated: October 30, 2026
1-Chloroethyl chloroformate → HCID 10332074, compound
https://huagongshe.com/reaction/1743864
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 10422650 | HCID 10422650 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 10332074 | HCID 10332074 | 69.4% |
Reaction Steps
To a solution of 8-fluoro-3-methyl-2,3,4,5,10,11-hexahydro-1H,9H-cyclopenta[b][1,4]diazocino[7,8,1-hi]indole (0.90 g, 3.48 mmole) in dichloroethane (200 mL) was added 1-chloroethyl chloroformate (1.5 mL, 13.8 mmole) and the mixture refluxed for 24 hours. The reaction mixture was then cooled to room temperature and the solvent removed in vacuo and replaced with methanol (200 mL) and refluxed for another 3 h. 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 0.59 g of the title compound as a white solid. 0.18 g of the above solid was further treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 199-200° C. MS (ES) m/z 245.11 ([M+H]+), MS (ES) m/z 286.14 ([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-3fd4f34a6ff24e109a420994a9184ff1 |
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| Source note | uspto-grants-2006_03 |
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