HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374107Generated: October 30, 2026
Methyl chloroformate → HCID 10598276, compound
https://huagongshe.com/reaction/374107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10428804 | HCID 10428804 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10598276 | HCID 10598276 | 65.6% |
Reaction Steps
To a solution of N-(1-benzyl-4-methylhexahydro-1H-1,4-diazepin-6-yl)-1H-indazole-3-carboxamide (0.92 g) and triethylamine (0.77 g) in dichloromethane (30 ml), methyl chloroformate (0.48 g) is added dropwise at 0° C., and the mixture is stirred at 25° C. for 16 hours. The reaction mixture is washed with saturated sodium bicarbonate and dried over sodium sulfate. The solvent is evaporated under reduced pressure, and the residue is chromatographed on silica gel with elution of acetone. Fractions containing the title compound are pooled and evaporated under reduced pressure to give the title compound (0.7 g) as an oil. The free base thus obtained is converted to the fumarate of the title compound in a usual manner, m.p. 158°-160° C. (recrystallized from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166341 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-79e3abdce53e42f798c4fee0b06035e6 |
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| Source note | uspto-grants-1992_11 |
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