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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524605Generated: October 31, 2026

(2R,3S)-2-methylmorpholine-3-carboxylic acid → (2R,3S)-4-((6-(2-chloro-4-fluorophenyl)-5-(methoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)-2-methylmorpholine-3-carboxylic acid

https://huagongshe.com/reaction/524605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R,3S)-2-methylmorpholine-3-carboxylic acidHCID 45791333—
Reactant6-Bromomethyl-4-(2-chloro-4-fluoro-phenyl)-2-thiazol-2-yl-1,4-dihydro-pyrimidine-5-carboxylic acid methyl esterHCID 89995963—
Product(2R,3S)-4-((6-(2-chloro-4-fluorophenyl)-5-(methoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)-2-methylmorpholine-3-carboxylic acidHCID 7329563852%

Reaction Steps

Methyl 6-(bromomethyl)-4-(2-chloro-4-fluorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (0.85 g, 1.9 mmol) was reacted with (2R,3S)-2-methylmorpholine-3-carboxylic acid (0.28 g, 1.9 mmol) according to the procedure as described in Example 34 to give the title compound as a yellow solid (0.5 g, 52%). 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-8fdc8a1e6ce84b5292c4b2002d38e320
Source noteuspto-grants-2016_05