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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428852Generated: October 30, 2026

Methanesulfonyl chloride → HCID 22141344, compound

https://huagongshe.com/reaction/428852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 22141239HCID 22141239—
SolventPyridineHCID 1049—
ProductHCID 22141344HCID 2214134450%

Reaction Steps

To a solution of 3-(3-benzyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenylamine (Preparation 30, 1.58 g, 5.68 mmol) in pyridine (10 ml) under nitrogen at 0° C. was added methanesulphonyl chloride (0.66 ml, 8.52 mmol) dropwise to the solution, and the mixture was stirred for 14 hours at room temperature. The pyridine was evaporated in vacuo and the residue was partitioned between dichloromethane (50 ml) and dilute aqueous sodium hydrogen carbonate solution (1 M, 50 ml). The layers were separated and the organic extract was dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by silica (60 g) column chromatography eluting with ethyl acetate:hexane (5:95) then ethyl iacetate:hexane:triethylamine (5:95:0.1 increasing to 80:20:0.1). Appropriate fractions were combined and concentrated in vacuo to give the title compound as an off-white solid (1 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313312B1
Source datasetuspto-grants-2001_11
ORD IDord-364ba59543de4fad913739811d1af6cf
Source noteuspto-grants-2001_11