Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176163Generated: October 31, 2026

5-Ethynyl-2-methylpyridine → HCID 45381859, compound

https://huagongshe.com/reaction/2176163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Ethynyl-2-methylpyridineHCID 638197—
ReactantHCID 67545385HCID 67545385—
ProductHCID 45381859HCID 45381859—

Reaction Steps

The coupling of 9-(trifluoromethoxy)-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole (140 mg, 0.473 mmol; Example 175) and 5-ethynyl-2-methylpyridine (111 mg, 0.945 mmol; prepared as described in International Publication No. WO2005090333) was performed according to the procedure described in Example 20 to afford the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 1.66-1.80 (m, 2H), 1.84-1.98 (m, 2H), 2.40 (s, 3H), 2.95-3.23 (m, 5H), 4.24 (s, 2H), 6.83 (d, J=8 Hz, 1H), 6.92-6.99 (m, 2H), 7.06-7.16 (m, 3H), 7.28 (s, 1H), 7.85 (s, 1H); MS (DCI/NH3) m/z 414 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09063126B2
Source datasetuspto-grants-2015_06
ORD IDord-2f91df7f28994dfabb4027f992ec7a44
Source noteuspto-grants-2015_06