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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176194Generated: October 25, 2026

7-Bromoquinoline → HCID 45381391, compound

https://huagongshe.com/reaction/2176194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-BromoquinolineHCID 521259—
ReactantHCID 67543761HCID 67543761—
ProductHCID 45381391HCID 45381391—

Reaction Steps

The reaction of 9-fluoro-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole (230 mg, 1.0 mmol; Example 161) and 7-bromoquinoline (312 mg, 1.5 mmol; Ark Pharm) was performed as described in Example 68 to afford the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 1.95-2.22 (m, 4H) 2.96-3.03 (m, 1H) 3.09-3.29 (m, 4H) 4.32 (s, 2H) 6.86 (td, J=9, 2 Hz, 1H) 7.07-7.17 (m, 2H) 7.58-7.67 (m, 2H) 7.97 (d, J=2 Hz, 1H) 8.18 (d, J=9 Hz, 1H) 8.50 (d, J=8 Hz, 1H) 8.95 (dd, J=4, 2 Hz, 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-9a45701991a746ad8a4618af5d4bd2f8
Source noteuspto-grants-2015_06