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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524638Generated: October 30, 2026

(S)-morpholine-3-carboxylic acid → (3S)-4-((5-(ethoxycarbonyl)-6-(5-fluoro-3',5'-bis(trifluoromethyl)-[1,1'-biphenyl]-2-yl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxylic acid

https://huagongshe.com/reaction/524638

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-morpholine-3-carboxylic acidHCID 1501894—
ReactantEthyl 6-(bromomethyl)-4-(5-fluoro-3',5'-bis(trifluoromethyl)-[1,1'-biphenyl]-2-yl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 118107610—
Product(3S)-4-((5-(ethoxycarbonyl)-6-(5-fluoro-3',5'-bis(trifluoromethyl)-[1,1'-biphenyl]-2-yl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxylic acidHCID 11810756458%

Reaction Steps

Ethyl 6-(bromomethyl)-4-(5-fluoro-3′,5′-bis(trifluoromethyl)-[1,1′-biphenyl]-2-yl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (3.37 g, 5.3 mmol) was reacted with (S)-morpholine-3-carboxylic acid (0.69 g, 5.3 mmol) according to the procedure described in Example 1, Step C to give the title compound as a yellow solid (2.11 g, 58%). 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-323cdfd358ec4f1a846ce118142550d4
Source noteuspto-grants-2016_05