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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524603Generated: November 1, 2026

(2R,3S)-2-methylmorpholine-3-carboxylic acid → (2R,3S)-4-((6-(2,4-dichlorophenyl)-5-(ethoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)-2-methylmorpholine-3-carboxylic acid

https://huagongshe.com/reaction/524603

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R,3S)-2-methylmorpholine-3-carboxylic acidHCID 45791333—
ReactantEthyl 6-(bromomethyl)-4-(2,4-dichlorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 118107510—
Product(2R,3S)-4-((6-(2,4-dichlorophenyl)-5-(ethoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)-2-methylmorpholine-3-carboxylic acidHCID 7329580242%

Reaction Steps

Ethyl 6-(bromomethyl)-4-(2,4-dichlorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (0.9 g, 1.9 mmol) was reacted with (2R,3S)-2-methyl morpholine-3-carboxylic acid (0.28 g, 1.9 mmol) according to the procedure as described in Example 34, Step D to give the title compound as a yellow solid (0.43 g, 42%). 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-4520f0cdfec041d29d28d68d58d11fb3
Source noteuspto-grants-2016_05