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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271885Generated: November 2, 2026

2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol → HCID 66716046, compound

https://huagongshe.com/reaction/2271885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 66715127—
ReactantHCID 66715507HCID 66715507—
ProductHCID 66716046HCID 6671604664%

Reaction Steps

Following general procedure D, (6-bromo-4-(4-(3-methoxypyrrolidin-1-yl)cyclohexylamino)quinolin-3-yl)(cyclopropyl)methanone (60 mg, 0.13 mmol) was reacted with 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (55 mg, 0.19 mmol) to afford the desired product (46 mg, 64%) as a brown solid: 1H NMR 1H NMR (500 MHz, MeOD+TFA-d) δ 9.42 (s, 1H), 8.46 (s, 1H), 8.31-8.23 (m, 1H), 8.04-7.97 (m, 1H), 7.75 (s, 1H), 7.71 (s, 1H), 4.99 (br s, 1H), 4.23-4.14 (m, 1H), 3.82-3.61 (m, 2H), 3.43-3.30 (m, 6H), 3.27-3.19 (m, 1H), 2.93-2.82 (m, 1H), 2.60-2.03 (m, 7H), 2.02-1.61 (m, 3H), 1.37-1.18 (m, 4H).; ESI MS m/z 554 [C30H33Cl2N3O3+H]+; HPLC>99.0% (AUC), tR=10.97 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-0f72b8bfd2854265a296e35c16d506b3
Source noteuspto-grants-2015_09