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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271746Generated: October 25, 2026

2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol → HCID 178484095, compound

https://huagongshe.com/reaction/2271746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 66715127—
ReactantHCID 178484093HCID 178484093—
ProductHCID 178484095HCID 17848409558.4%

Reaction Steps

Following general procedure F, {6-bromo-4-[trans-4-(dimethylamino)cyclohexylamino]quinolin-3-yl}(cyclopropyl)methanone (45 mg, 0.110 mmol) was reacted with 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (38 mg, 0.135 mmol) to afford the desired product (32 mg, 58%) as a light yellow solid: NMR (500 MHz, CD3OD) δ 9.30 (s, 1H), 8.50 (s, 1H), 8.28 (d, J=8.8 Hz, 1H), 8.00 (d, J=8.8 Hz, 1H), 7.78 (s, 2H), 4.47 (s, 1H), 3.45 (s, 1H), 2.91 (s, 6H), 2.85 (s, 1H), 2.51 (s, 2H), 2.31 (s, 2H), 1.91-1.74 (m, 4H), 1.31-1.18 (m, 4H); ESI MS m/z 498 [C27H29Cl2N3O2+H]+; HPLC 96.9% (AUC), tR=11.50 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-f8b5a15ab9b341aab3ccadfe58a2ab7c
Source noteuspto-grants-2015_09