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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500707Generated: October 31, 2026

N-bromobutanimide → 3-(4-Bromo-2-fluoro-phenylamino)-5-formylaminomethyl-pyrazine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1500707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 59140179HCID 59140179—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-(4-Bromo-2-fluoro-phenylamino)-5-formylaminomethyl-pyrazine-2-carboxylic acid methyl esterHCID 5914017680.1%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a −30° C. solution of 3-(2-fluoro-4-trimethylsilanyl-phenylamino)-5-formylaminomethyl-pyrazine-2-carboxylic acid methyl ester (1.84 g, 4.89 mmol) in dichloromethane (50 mL) under N2 was added NBS (0.96 g, 5.38 mmol, 1.1 eq.), and the reaction mixture was stirred at −30° C. for 3 h. More NBS (0.96 g, 5.38 mmol, 1.1 eq.) was added, and the reaction mixture was allowed to stand at 0° C. for 18 h. The reaction mixture was diluted with ethyl acetate (250 mL). The organic layer was washed with saturated aqueous solution of sodium bicarbonate, water and brine, dried (Na2SO4), filtered and concentrated in vacuo. The crude material was triturated with methanol to afford the desired product as a yellow solid (1.50 g, 80.1%). LCMS (method C): RT=2.51 min, [M+H]+=383/384.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206174B2
Source datasetuspto-grants-2015_12
ORD IDord-e8f8af97c83a49718a9c86d377a5886f
Source noteuspto-grants-2015_12