Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229783Generated: October 26, 2026

Pyridine-2-sulfonic acid allyl-(2-methyl-pent-4enyl)-amide → 3-Methyl-1-(pyridine-2-sulfonyl)-2,3,4,7-tetrahydro-1H-azepine

https://huagongshe.com/reaction/229783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine-2-sulfonic acid allyl-(2-methyl-pent-4enyl)-amideHCID 11565389—
CatalystHCID 178479819HCID 178479819—
SolventDichloromethaneHCID 6344—
Product3-Methyl-1-(pyridine-2-sulfonyl)-2,3,4,7-tetrahydro-1H-azepineHCID 1163022383%

Reaction Steps

Pyridine-2-sulfonic acid allyl-(2-methyl-pent-4-enyl)-amide (1.2 g, 4.3 mmol) was diluted in CH2Cl2 (100 ml). After carefully degass by Ar, Grubbs catalyst (0.35 g, 0.43 mmol) was added under Ar protection. The mixture was then refluxed for 2 h before the reaction mixture was concentrated by rotary evaporation. The product was purified by column chromatography (5%-20% EtOAc/hexanes) to give the title compound (0.9 g, 83% yield): MS (M+H+):253.2; 1H-NMR (400 Hz, CDCl3): d=8.70(d, 1H), 8.0-7.75(m, 2H), 7.5 (m, 1H) 5.79-5.60(m, 2H), 4.00(d, 2H), 3.65(dd, 1H), 3.22(dd, 1H), 2.30-2.05(m, 3H), 0.96(d, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563784B2
Source datasetuspto-grants-2009_07
ORD IDord-a3ea2d4def5041b6a36644d1314d6122
Source noteuspto-grants-2009_07