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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524828Generated: October 30, 2026

(S)-2-((tert)-Butoxycarbonyl)amino)butanoic acid → Ethyl 6-(((R)-3-((((S)-2-aminobutanoyl)oxy)methyl)morpholino)methyl)-4-(2-bromo-4-fluorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/524828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-((tert)-Butoxycarbonyl)amino)butanoic acidHCID 2755934—
ReactantEthyl 4-(2-bromo-4-fluorophenyl)-6-(((S)-3-(hydroxymethyl)morpholino)methyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 118107606—
ProductEthyl 6-(((R)-3-((((S)-2-aminobutanoyl)oxy)methyl)morpholino)methyl)-4-(2-bromo-4-fluorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 11810750631.2%

Reaction Steps

Ethyl 4-(2-bromo-4-fluorophenyl)-6-(((S)-3-(hydroxymethyl)morpholino)methyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (1 g, 1.9 mmol) was reacted with (S)-2-((tert-butoxycarbonyl)amino)butanoic acid (0.61 g, 3 mmol) according to the procedure as described in Example 49 to give the title compound as yellow oil (0.37 g, 31%). 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-0cf949683c644b04b6c2f5ba6b4ed1bb
Source noteuspto-grants-2016_05