Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271759Generated: November 1, 2026

3-Chloro-4-hydroxyphenylboronic Acid → HCID 66716406, compound

https://huagongshe.com/reaction/2271759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-hydroxyphenylboronic AcidHCID 22125373—
ReactantHCID 66715275HCID 66715275—
ProductHCID 66716406HCID 6671640657.9%

Reaction Steps

Following general procedure D, {6-bromo-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]quinolin-3-yl}(cyclopropyl)methanone (30 mg, 0.065 mmol) was reacted with 3-chloro-4-hydroxyphenylboronic acid (26 mg, 0.150 mmol) to afford the desired product (19 mg, 57%) as a yellow solid: 1H NMR (500 MHz, CD3OD) δ 8.76 (s, 1H), 8.28 (s, 1H), 8.06-7.98 (m, 2H), 7.71 (d, J=2.3 Hz, 1H), 7.54 (dd, J=8.4, 2.3 Hz, 1H), 7.09-7.03 (m, 1H), 3.55 (d, J=12.8 Hz, 2H), 3.34 (s, 3H), 3.23-3.15 (m, 2H), 2.81-2.50 (m, 8H), 2.35 (s, 3H), 2.12 (d, J=10.6 Hz, 2H), 1.92-1.81 (m, 2H), 1.34-1.28 (m, 2H), 1.27-1.20 (m, 2H); ESI MS m/z 505 [C29H33ClN4O4+H]+; HPLC>99% (AUC), tR=10.01 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-d505b8794a634965a226763bbe6a6996
Source noteuspto-grants-2015_09