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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374730Generated: October 26, 2026

Hexahydro-1H-azepine-1-ethanamine → N-(2-azepan-1-ylethyl)-N-{4-[2-(3-chlorophenyl)-6-(trifluoromethyl)pyrazolo[1,5-a]pyridin-3-yl]pyrimidin-2-yl}amine

https://huagongshe.com/reaction/1374730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexahydro-1H-azepine-1-ethanamineHCID 40002—
Reactant4-[2-(3-Chlorophenyl)-6-(trifluoromethyl)pyrazolo[1,5-a]pyridin-3-yl]pyrimidin-2-yl methyl sulfoneHCID 17962380—
SolventWaterHCID 962—
ProductN-(2-azepan-1-ylethyl)-N-{4-[2-(3-chlorophenyl)-6-(trifluoromethyl)pyrazolo[1,5-a]pyridin-3-yl]pyrimidin-2-yl}amineHCID 10207930—

Reaction Steps

2-Azepan-1-ylethylamine (0.04 mL) and 4-[2-(3-chlorophenyl)-6-(trifluoromethyl)pyrazolo[1,5-a]pyridin-3-yl]pyrimidin-2-yl methyl sulfone (0.02 g) were mixed at room temperature and heated with an airgun until a homogenous melt was obtained (2 min). Upon cooling, water was added. The precipitated solid was filtered and dried to give the title compound as a beige solid (0.014 g); 1H NMR (d6-DMSO) δ 9.51(1H, s), 8.49(1H, bs), 8.16(1H, d), 7.70–7.65(2H, m), 7.60–7.50(3H, m), 7.00(1H, bs), 6.36(1H, bs), 2.6(6H, bs), 1.6(8H, bs); m/z 515(M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166597B2
Source datasetuspto-grants-2007_01
ORD IDord-cb0a0c3edb904cf59a39895d15da4c7b
Source noteuspto-grants-2007_01