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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076193Generated: November 1, 2026

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

https://huagongshe.com/reaction/2076193

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 numberUS07923456B2
Source datasetuspto-grants-2011_04
ORD IDord-f23a568aeb424fe9b01c8c973186f84b
Source noteuspto-grants-2011_04