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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72445Generated: October 29, 2026

Triethylamine → Methyl 5-chloro-2-(3-((2,4-difluorophenyl)amino)azetidin-1-yl)nicotinate

https://huagongshe.com/reaction/72445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 2,5-DichloronicotinateHCID 2764318—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantTert-butyl 3-((2,4-difluorophenyl)amino)azetidine-1-carboxylateHCID 63303164—
SolventDichloromethaneHCID 6344—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductMethyl 5-chloro-2-(3-((2,4-difluorophenyl)amino)azetidin-1-yl)nicotinateHCID 6795802542.5%

Reaction Steps

To a cooled (0° C.) solution of tert-butyl 3-((2,4-difluorophenyl)amino)azetidine-1-carboxylate (D31) (90 mg, 0.316 mmol) in dichloromethane, a mixture of trifluoroacetic acid/dichloromethane (3 ml/1 ml) was added and the reaction mixture was stirred 1 h. The solvents were evaporated in vacuo and the residue was dissolved in tetrahydrofuran/methanol (3/1 ml) triethylamine (0.132 ml, 0.95 mmol) was added followed by the addition of methyl 2,5-dichloronicotinate (52.33 mg, 0.253 mmol) and the resulting mixture was stirred 12 h at 75° C. The residue abtained after solvent evaporation was purified by Biotage SNAP-Si column eluting with cyclohexane/ethyl acetate from 100/0 to 90/10. Collected fractions afforded the title compound (D85) (0022/086/5) (38 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828987B2
Source datasetuspto-grants-2014_09
ORD IDord-13b22ee979534379850a65b42e3ebcf9
Source noteuspto-grants-2014_09