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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271847Generated: November 2, 2026

2-Chloro-6-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol → HCID 66716276, compound

https://huagongshe.com/reaction/2271847

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 66716079—
ReactantHCID 86692873HCID 86692873—
ProductHCID 66716276HCID 6671627631.5%

Reaction Steps

Following general procedure D, [1-(6-bromo-4-(6-(4-methylpiperazin-1-yl)pyridin-3-ylamino)quinolin-3-yl)ethanone (50 mg, 0.113 mmol) was reacted with 2-chloro-6-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (34 mg, 0.124 mmol) to afford the desired product (18 mg, 31%) as a yellow-orange solid: 1H NMR (500 MHz, CD3OD) δ 9.08 (s, 1H), 8.07 (d, J=3 Hz, 1H), 7.91 (s, 2H), 7.82 (s, 1H), 7.49 (dd, J=12, 2.0 Hz, 1H), 7.00-6.92 (m, 3H), 3.66 (t, J=10 Hz, 4H), 2.77 (s, 3H), 2.62 (t, J=10 Hz, 4H), 2.39 (s, 3H); ESI MS m/z 506, [C27H25ClFN5O2+H]+; HPLC 98.9% (AUC), tR=14.39 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-4cdcadd99d0146e5be658caadb7d81c0
Source noteuspto-grants-2015_09