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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845637Generated: October 31, 2026

Chloroform → HCID 53987743, compound

https://huagongshe.com/reaction/845637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantMethyl chloroformateHCID 6586—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178477868HCID 178477868—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53987743HCID 53987743—

Reaction Steps

To a stirred suspension of 5.8 g of 6-chloro-3-(4-piperidinyl)-1H-indazole, 4.6 g of sodium bicarbonate and trichloromethane (25 ml)-tetrahydrofuran (25 ml) was added, dropwise, 5.2 g of methyl chloroformate. The reaction mixture was stirred at ambient temperature for 16 hrs and then poured into water. The organic layer was collected, washed with water, dried over anhydrous potassium carbonate and the solvent concentrated to give 4-(6-chloro-1-methyoxycarbonyl-1H-indazol-3-yl)piperidine-1-carboxylic acid methyl ester, as an oil. The oil was dissolved in 50 ml of methanol and 1.5 ml of a 25% sodium methoxide-methanol solution was added. The reaction mixture was stirred at ambient temperature for 0.5 hrs, poured into water and the aqueous mixture extracted with dichloromethane. The dichloromethane extract was washed with water, dried over anhydrous magnesium sulfate and the solvent evaporated to an oil. The oil was triturated with hexane. Recrystallization from toluene-hexane (twice) yielded 3.5 g (47%) of product, mp 132-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04758668
Source datasetuspto-grants-1988_07
ORD IDord-a7703996bffc4a9d967742faf64a7528
Source noteuspto-grants-1988_07