Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466454Generated: October 27, 2026

Triethylamine → Methyl 1-{[(5-bromo-2-methylphenyl)acetyl]amino}cyclohexanecarboxylate

https://huagongshe.com/reaction/1466454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantMethyl 1-aminocyclohexane-1-carboxylate hydrochlorideHCID 22645079—
Reactant2-(5-Bromo-2-methylphenyl)acetic acidHCID 51063743—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductMethyl 1-{[(5-bromo-2-methylphenyl)acetyl]amino}cyclohexanecarboxylateHCID 67375467—

Reaction Conditions

Temperature80 °C

Reaction Steps

2.06 g (9.00 mmol) of (5-bromo-2-methylphenyl)acetic acid (described in EP 1791816 and WO 2006/29799) were dissolved in 3.7 ml (51.3 mmol) of thionyl chloride. The reaction mixture was stirred at 80° C. for 2 h and then concentrated. The residue was dissolved in 20 ml of dichloromethane. 2.09 g (10.8 mmol) of methyl 1-aminocyclohexanecarboxylate hydrochloride were dissolved in 25 ml of dichloromethane, 55 mg (0.45 mmol) of 4-dimethylaminopyridine and 3.1 ml (22.5 mmol) of triethylamine were added and the mixture was stirred at room temperature for 0.5 h. The solution of the acid chloride was added dropwise, and the mixture was stirred at room temperature for 36 h. The mixture was then diluted with diluted with dichloromethane, washed with water, 1N aqueous hydrogen chloride solution and saturated aqueous sodium bicarbonate solution, dried, filtered and concentrated. This gave 2.80 g (84% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000026B2
Source datasetuspto-grants-2015_04
ORD IDord-3f84aaa80efa41e0b15a4df8dae3af7a
Source noteuspto-grants-2015_04