Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524718Generated: October 30, 2026

N-bromobutanimide → Ethyl 6-(bromomethyl)-4-(2-chloro-4-fluorophenyl)-2-(3-fluoro pyridin-2-yl)-1,4-dihydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/524718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 4-(2-chloro-4-fluorophenyl)-2-(3-fluoropyridin-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylateHCID 9930383—
ProductEthyl 6-(bromomethyl)-4-(2-chloro-4-fluorophenyl)-2-(3-fluoro pyridin-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 11810753862%

Reaction Steps

Ethyl 4-(2-chloro-4-fluorophenyl)-2-(3-fluoropyridin-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate (3 g, 7.7 mmol) was reacted with NBS (1.51 g, 8.47 mmol) according to the procedure as described in Example 1, Step B to give the title compound as a yellow solid (2.2 g, 62%). 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-bb1352a17b0646b4b35a2efd053184b9
Source noteuspto-grants-2016_05