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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271955Generated: November 2, 2026

2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol → HCID 66715555, compound

https://huagongshe.com/reaction/2271955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 66715127—
Reactant{6-Bromo-4-[6-(pyrrolidin-1-ylmethyl)pyridin-3-ylamino]quinolin-3-yl}(cyclopropyl)methanoneHCID 66715896—
ProductHCID 66715555HCID 6671555564%

Reaction Steps

Following general procedure F, {6-Bromo-4-[6-(pyrrolidin-1-ylmethyl)pyridin-3-ylamino]quinolin-3-yl}(cyclopropyl)methanone (45 mg, 0.100 mmol) was reacted with 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (43 mg, 0.150 mmol) to afford the desired product (34 mg, 64%) as a yellow solid: 1H NMR (500 MHz, CD3OD+TFA-d) δ 9.40 (s, 1H), 8.72 (d, J=2.5 Hz, 1H), 8.30 (dd, J=8.8, 2.0 Hz, 1H), 8.16-8.06 (m, 2H), 7.96 (dd, J=8.3, 2.5 Hz, 1H), 7.65 (d, J=8.3 Hz, 1H), 7.46 (s, 2H), 4.65 (s, 2H), 3.63-3.59 (m, 2H), 3.21-3.12 (m, 2H), 2.85-2.76 (m, 1H), 2.20-2.16 (m, 2H), 2.09-2.01 (m, 2H), 1.20-1.10 (m, 4H); ESI MS m/z 533 [C29H26Cl2N4O2+H]+; HPLC 98.8% (AUC), tR=10.76 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-859a0623a50b4bbbb30f00d82add081b
Source noteuspto-grants-2015_09