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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176191Generated: October 26, 2026

7-Bromoisoquinoline → HCID 45381394, compound

https://huagongshe.com/reaction/2176191

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-BromoisoquinolineHCID 12257441—
Reactant9-fluoro-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indoleHCID 67543761—
ProductHCID 45381394HCID 45381394—

Reaction Steps

The reaction of 9-fluoro-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole (78 mg, 0.34 mmol; Example 161) and 7-bromoisoquinoline (106 mg, 0.51 mmol; Frontier) was performed as described in Example 68 to afford the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 1.94-2.22 (m, 4H) 2.88-2.96 (m, 1H) 3.08-3.29 (m, 4H) 4.31 (s, 2H) 6.85 (td, J=9, 2 Hz, 1H) 7.06 (dd, J=9, 4 Hz, 1H) 7.12 (dd, J=10, 2 Hz, 1H) 7.74 (dd, J=9, 2 Hz, 1H) 7.96 (d, J=6 Hz, 1H) 8.13 (d, J=2 Hz, 1H) 8.17 (d, J=8 Hz, 1H) 8.55 (d, J=6 Hz, 1H) 9.35 (s, 1H); MS (DCI/NH3) m/z 358 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09063126B2
Source datasetuspto-grants-2015_06
ORD IDord-2b12888dc1024feaba7533b61129d4f9
Source noteuspto-grants-2015_06