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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711246Generated: October 27, 2026

4-Amino-3-bromobenzamide → 4-Amino-3-(4,4-dimethyl-cyclohex-1-enyl)-benzamide

https://huagongshe.com/reaction/1711246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3-bromobenzamideHCID 12118055—
Reactant2-(4,4-Dimethylcyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 23142013—
SolventDichloromethane methanolHCID 21226129—
Product4-Amino-3-(4,4-dimethyl-cyclohex-1-enyl)-benzamideHCID 5875485878%

Reaction Steps

The title compound was prepared by the Suzuki coupling procedure of Example 11, step (e) using 4-amino-3-bromo-benzamide (as prepared in Example 16, step (a), 62.4 mg, 0.289 mmol), and 2-(4,4-dimethyl-cyclohex-1-enyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (75.0 mg, 0.318 mmol). Silica gel chromatography (0-2% MeOH/DCM) afforded the title compound (55 mg, 78%) as a faint yellow solid. Mass spectrum (ESI, m/z): Calcd. for C15H20N2O, 245.2 (M+H), found 245.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790724B2
Source datasetuspto-grants-2010_09
ORD IDord-3ca54e532cfb4baaa87bd9cbae713f31
Source noteuspto-grants-2010_09