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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524805Generated: October 31, 2026

N-bromobutanimide → Ethyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(5-methoxy thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/524805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 4-(2-bromo-4-fluorophenyl)-2-(5-methoxythiazol-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylateHCID 90042921—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(5-methoxy thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 9004300934.1%

Reaction Steps

Ethyl 4-(2-bromo-4-fluorophenyl)-2-(5-methoxythiazol-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate (2 g, 4.4 mmol) was reacted with NBS (0.78 g, 4.4 mmol) in DCM (50 mL) according to the procedure as described in Example 1, Step B to give the title compound as a yellow solid (0.80 g, 34%). The compound was characterized by the following spectroscopic data:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340538B2
Source datasetuspto-grants-2016_05
ORD IDord-381fed4a72e9496a885fe92997626370
Source noteuspto-grants-2016_05