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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397707Generated: October 29, 2026

Pyridine → HCID 23001032, compound

https://huagongshe.com/reaction/397707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 23000931HCID 23000931—
SolventDichloromethaneHCID 6344—
ProductAmmoniaHCID 222—
ProductHCID 23001032HCID 23001032136.6%

Reaction Steps

To 4-(3-aminophenyl)-N-hexyl-4-methylpiperidine (Preparation 56, 70.0 mg, 0.27 mmol) in dichloromethane (3 ml) was added methanesulfonyl chloride (61 mg, 0.53 mmol) in dichloromethane (0.5 ml) and pyridine (42 mg, 0.53 mmol) in dichloromethane (0.5 ml) at room temperature. The solution was stirred at room temperature for 16 h, then it was concentrated in vacuo to give the crude product. This was purified by silica column chromatography eluting with a gradient of ethyl acetate:hexane:0.88 ammonia (90:10:1 to 98:2:1) to give the title compound as a colourless oil (65 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610711B2
Source datasetuspto-grants-2003_08
ORD IDord-561c5c0b599c4d02a44cc86961f14376
Source noteuspto-grants-2003_08