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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464047Generated: October 29, 2026

Dichloromethane → HCID 13306782, compound

https://huagongshe.com/reaction/464047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCyanogen BromideHCID 10476—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 20263914HCID 20263914—
ProductHCID 13306782HCID 1330678258%

Reaction Steps

To a solution of 1-[2-(4-methoxyphenyl)ethyl]-4-ethyl-4-(1H-pyrrol-1-yl)aminopiperidine of Example 12a (4 g, 13.4 mmole) in 150 ml dichloromethane containing sodium bicarbonate (3.4 g, 40 mmole) was added a solution of cyanogen bromide (1.6 g, 14.7 mmole) in 25 ml dichloromethane. After stirring twenty hours at ambient temperature, the reaction mixture was evaporated, stirred with water and extracted with ether. The organic extract was washed with water and saturated NaCl and was dried (anhydrous MgSO4), filtered and evaporated to 5 g of an oil. The oil was converted to the hydrochloride salt as in Example 2 and was recrystallized from isopropanol-ether to give 2.8 g (58%) of N-{1-[2-(4-methoxyphenyl)ethyl]piperidin-4-yl}-N-(1H-pyrrol-1-yl)cyanamide hydrochloride, d 227°-229° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04546105
Source datasetuspto-grants-1985_10
ORD IDord-ffdda5ae943b424290423675d2c20ff5
Source noteuspto-grants-1985_10