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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595495Generated: October 29, 2026

Bromotrichloromethane → Ethyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)oxazole-4-carboxylate

https://huagongshe.com/reaction/595495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrichloromethaneHCID 6383—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantMethyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-4,5-dihydrooxazole-4-carboxylateHCID 89689795—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)oxazole-4-carboxylateHCID 89689616—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of methyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-4,5-dihydrooxazole-4-carboxylate (37) (100 mg, 0.336 mmol) in DCM (20 mL), DBU (1.008 mmol) and bromotrichloromethane (0.403 mmol) were added at 0° C. and stirred the reaction mixture for 2 h at 0° C. Reaction temperature was raised to room temperature and stirred the reaction for 10 min. The reaction mixture was diluted with DCM and washed with water, 10% NaHCO3 solution and brine solution. The organic layer was collected, dried over Na2SO4, filtered and concentrated. The crude material obtained was purified by flash chromatography using silica gel and EtOAC:pet ether as eluent to afford the title compound, ethyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)oxazole-4-carboxylate (38). 1H NMR: 400 MHz, DMSO-d6: δ 1.24-1.27 (m, 6H), 3.87 (s, 3H), 3.92-3.97 (m, 1H), 6.92 (s, 1H), 8.36 (d, J=7.60 Hz, 1H), 8.60 (s, 1H), 9.00 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242976B2
Source datasetuspto-grants-2016_01
ORD IDord-48a2ae475bbf421d9c56943b4586b604
Source noteuspto-grants-2016_01