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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271757Generated: November 2, 2026

2-Chloro-6-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol → HCID 178487412, compound

https://huagongshe.com/reaction/2271757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 17750230—
ReactantHCID 178519796HCID 178519796—
ProductHCID 178487412HCID 17848741267%

Reaction Steps

Following general procedure D, {6-bromo-4-[trans-4-(pyrrolidin-1-yl)cyclohexylamino]quinolin-3-yl}(cyclopropyl)methanone (25 mg, 0.150 mmol) was reacted with 2-chloro-6-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (43 mg, 0.150 mmol) to afford the desired product (20 mg, 67%), as a yellow-brown solid: 1H NMR (500 MHz, CD3OD) δ 9.14 (s, 1H), 8.34 (d, J=1.9 Hz, 1H), 8.03 (dd, J=8.7, 1.9 Hz, 1H), 7.92 (d, J=8.7 Hz, 1H), 7.29 (d, J=2.1 Hz, 1H), 7.22 (d, J=2.0 Hz, 1H), 4.15 (t, J=10.6 Hz, 1H), 3.99 (s, 3H), 3.16 (s, 4H), 2.94 (s, 1H), 2.89-2.79 (m, 1H), 2.38 (d, J=12.5 Hz, 2H), 2.28 (d, J=11.9 Hz, 2H), 1.99 (s, 4H), 1.70-1.50 (m, 4H), 1.23-1.17 (m, 2H), 1.13-1.06 (m, 2H); ESI MS m/z 520 [C30H34ClN3O3+H]+; HPLC 98.7% (AUC), tR=10.99 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-a3d6acbadadf482f9588e521c535d211
Source noteuspto-grants-2015_09