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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524651Generated: October 31, 2026

(S)-morpholine-3-carboxylic acid → (3S)-4-((6-(2-bromo-4-fluorophenyl)-5-(ethoxycarbonyl)-2-(4-(2-(methylamino)-2-oxoethyl)thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxylic acid

https://huagongshe.com/reaction/524651

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-morpholine-3-carboxylic acidHCID 1501894—
ReactantEthyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(4-(2-(methyl amino)-2-oxoethyl)thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 118107552—
Product(3S)-4-((6-(2-bromo-4-fluorophenyl)-5-(ethoxycarbonyl)-2-(4-(2-(methylamino)-2-oxoethyl)thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxylic acidHCID 9004365253%

Reaction Steps

Ethyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(4-(2-(methylamino)-2-oxoethyl)thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (1.15 g, 2 mmol) was reacted with (S)-morpholine-3-carboxylic acid (0.39 g, 3 mmol) according to the procedure as described in Example 1, Step C to give the title compound as a yellow solid (0.66 g, 53%). 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-442eca40a5e9416198dad892b99dbcd5
Source noteuspto-grants-2016_05