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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176184Generated: October 31, 2026

7-Bromoisoquinoline → HCID 45381506, compound

https://huagongshe.com/reaction/2176184

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-BromoisoquinolineHCID 12257441—
ReactantHCID 67544841HCID 67544841—
ProductHCID 45381506HCID 45381506—

Reaction Steps

The reaction of 9-methyl-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole (226 mg, 1.0 mmol; Example 2B) and 7-bromoisoquinoline (312 mg, 1.5 mmol; Frontier) was performed as described in Example 68 to afford the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 1.94-2.20 (m, 4H) 2.42 (s, 3H) 2.91-2.98 (m, 1H) 3.08-3.29 (m, 4H) 4.32 (s, 2H) 6.90-6.96 (m, 1H) 6.98-7.04 (m, 1H) 7.22 (s, 1H) 7.73 (dd, J=8, 2 Hz, 1H) 7.94 (d, J=6 Hz, 1H) 8.09 (d, J=2 Hz, 1H) 8.15 (d, J=9 Hz, 1H) 8.53 (d, J=6 Hz, 1H) 9.33 (s, 1H); MS (DCI/NH3) m/z 354 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09063126B2
Source datasetuspto-grants-2015_06
ORD IDord-9dc1bff11be34a43af1bd481faa1011d
Source noteuspto-grants-2015_06