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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37802Generated: October 28, 2026

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline → HCID 53251425, compound

https://huagongshe.com/reaction/37802

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolineHCID 16217784—
Reactant7-bromo-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indoleHCID 67240163—
ProductHCID 53251425HCID 53251425—

Reaction Steps

7-Bromo-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole (146 mg, 0.5 mmol, Example 1B) was coupled with 6-quinolineboronic acid pinacol ester (191 mg, 0.75 mmol, Aldrich) following the procedure described in Example 4. Purification by preparative reverse-phase HPLC [Waters XBridge™ RP18 column, 5 μm, 30×100 mm, flow rate 40 mL/minute, 40-99% gradient of methanol in buffer (0.1 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] gave the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 1.99-2.18 (m, 4 H) 3.02-3.30 (m, 5 H) 4.29 (s, 2 H) 7.10-7.24 (m, 2 H) 7.36 (d, J=8 Hz, 1 H) 7.58 (dd, J=8, 4 Hz, 1 H) 8.04-8.10 (m, 1 H) 8.13-8.22 (m, 2 H) 8.45 (d, J=8 Hz, 1 H) 8.86 (dd, J=4, 2 Hz, 1 H); MS (DCI/NH3) m/z 340 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524703B2
Source datasetuspto-grants-2013_09
ORD IDord-38c701269cb746cf8776851c270e196f
Source noteuspto-grants-2013_09