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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051186Generated: October 31, 2026

Methyl chloroformate → HCID 10598276, compound

https://huagongshe.com/reaction/2051186

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 numberUS05017573
Source datasetuspto-grants-1991_05
ORD IDord-f6257c80fe9b45d889357d129388f242
Source noteuspto-grants-1991_05