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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826336Generated: November 2, 2026

Pyridine → HCID 22141217, compound

https://huagongshe.com/reaction/1826336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPyridine-3-sulfonyl chlorideHCID 3164136—
Reactant3-(3-Hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenylamineHCID 22141322—
SolventDichloromethaneHCID 6344—
ProductHCID 22141217HCID 2214121760%

Reaction Steps

To a solution of 3-(3-hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenylamine (Preparation 12, 220 mg, 0.809 mmol) in dichloromethane (5 ml) at room temperature was added pyridine (0.196 ml, 2.42 mmol) then dropwise over 5 minutes 3-pyridinesulfonylchloride (198 mg, 1.21 mmol). The mixture was stirred for 48 hours, concentrated in vacuo and the residue was purified by silica (10 g) column chromatography eluting with ethyl acetate then 90:10:1 ethyl acetate:methanol:ammonia solution (0.880). Product-containing fractions were combined and concentrated in vacuo to give the title compound as a pale orange oil (200 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049444B2
Source datasetuspto-grants-2006_05
ORD IDord-769a57f367b94a0b991aac66600cd29d
Source noteuspto-grants-2006_05