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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176162Generated: October 29, 2026

3-Ethynylpyridine → HCID 45381860, compound

https://huagongshe.com/reaction/2176162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-EthynylpyridineHCID 186003—
ReactantHCID 67545385HCID 67545385—
ProductHCID 45381860HCID 45381860—

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 3-ethynylpyridine (97 mg, 0.945 mmol; Aldrich) was performed according to the procedure described in Example 20 to afford the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 2.09-2.18 (m, 4H), 3.03-3.16 (m, 2H), 3.19-3.29 (m, 2H), 3.42-3.49 (m, 1H), 4.25 (s, 2H), 6.86 (d, J=14 Hz, 1H), 7.10 (ddd, J=9, 2, 1 Hz, 1H), 7.28 (d, J=1 Hz, 1H), 7.45 (dd, J=8, 5 Hz, 1H), 7.72 (d, J=9 Hz, 1H), 7.79 (d, J=15 Hz, 1H), 8.10 (dt, J=8, 2 Hz, 1H), 8.43 (dd, J=5, 2 Hz, 1H), 8.71 (d, J=2 Hz, 1H); MS (DCI/NH3) m/z 400 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09063126B2
Source datasetuspto-grants-2015_06
ORD IDord-103fd6fe37ba42939afe5bb19101b892
Source noteuspto-grants-2015_06