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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374107Generated: October 30, 2026

Methyl chloroformate → HCID 10598276, compound

https://huagongshe.com/reaction/374107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
ReactantHCID 10428804HCID 10428804—
SolventDichloromethaneHCID 6344—
ProductHCID 10598276HCID 1059827665.6%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166341
Source datasetuspto-grants-1992_11
ORD IDord-79e3abdce53e42f798c4fee0b06035e6
Source noteuspto-grants-1992_11