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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524587Generated: October 27, 2026

(S)-6,6-dimethylmorpholine-3-carboxylic acid hydrochloride → (3S)-4-((6-(2-chloro-4-fluorophenyl)-5-(ethoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)-6,6-dimethylmorpholine-3-carboxylic acid

https://huagongshe.com/reaction/524587

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-6,6-dimethylmorpholine-3-carboxylic acid hydrochlorideHCID 53487570—
ReactantEthyl 6-(bromomethyl)-4-(2-chloro-4-fluorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 118107632—
Product(3S)-4-((6-(2-chloro-4-fluorophenyl)-5-(ethoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)-6,6-dimethylmorpholine-3-carboxylic acidHCID 11810751159%

Reaction Steps

Ethyl 6-(bromomethyl)-4-(2-chloro-4-fluorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (0.26 g, 0.51 mmol) was reacted with (S)-6,6-dimethylmorpholine-3-carboxylic acid hydrochloride (0.1 g, 0.51 mmol) according to the procedure described in Example 1, Step C to give the title compound as a yellow solid (0.16 g, 59%). 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-62db138054e74849bee04d4c6b5f45f6
Source noteuspto-grants-2016_05