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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722143Generated: November 2, 2026

Chloroform → HCID 53987743, compound

https://huagongshe.com/reaction/1722143

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 numberUS04853470
Source datasetuspto-grants-1989_08
ORD IDord-6d0027d99ca648248d19c26c1a922eab
Source noteuspto-grants-1989_08