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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245300Generated: October 30, 2026

N-bromobutanimide → HCID 59432132, compound

https://huagongshe.com/reaction/245300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantN,N-Diethylethanamine trihydrofluorideHCID 175505—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-ethenyl-6-methoxycarbonylpyrimidineHCID 59432122—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59432132HCID 5943213244.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-vinyl-pyrimidine-4-carboxylic acid methyl ester (0.611 g, 1.809 mmol) and N-bromosuccinimide (0.386 g, 2.171 mmol) were dissolved in dichloromethane (10 ml) and the reaction mixture was cooled to 0° C. Triethylamine trihydrofluoride (0.884 mL, 5.43 mmol) was then added dropwise and the reaction mixture was allowed to warm to ambient temperature and stirred overnight. Water and additional dichloromethane were added. Sodium bicarbonate (0.760 g, 9.05 mmol) was added in several portions until no further gas evolution was noted. The organic phase was dried and concentrated under vacuum. The product was purified by flash chromatography on silica gel twice (first with dichloromethane/ethyl acetate gradient followed by hexane/ethyl acetate gradient) to provide the title compound (352 mg, 0.806 mmol, 44.6% yield) as a white solid, mp 144-146° C.: 1H NMR (CDCl3) δ 7.67 (dd, 1H), 7.23 (dd, 1H), 6.32 (ddd, 1H), 5.77 (br s, 2H), 4.01 (s, 3H), 4.0 (d, 3H), 3.77-3.94 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658791B2
Source datasetuspto-grants-2014_02
ORD IDord-8974ff19dc2b46cbabe3a09e0d8c6a03
Source noteuspto-grants-2014_02