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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524711Generated: October 31, 2026

2-(Morpholin-2-yl)acetic acid hydrochloride → 2-(4-((6-(2-bromo-4-fluorophenyl)-2-(1-(2-ethoxy-2-oxoethyl)-1H-1,2,4-triazol-3-yl)-5-(ethoxycarbonyl)-3,6-dihydropyrimidin-4-yl)methyl)morpholin-2-yl)acetic acid

https://huagongshe.com/reaction/524711

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Morpholin-2-yl)acetic acid hydrochlorideHCID 45259920—
ReactantEthyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(1-(2-ethoxy-2-oxoethyl)-1H-1,2,4-triazol-3-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 118107556—
Product2-(4-((6-(2-bromo-4-fluorophenyl)-2-(1-(2-ethoxy-2-oxoethyl)-1H-1,2,4-triazol-3-yl)-5-(ethoxycarbonyl)-3,6-dihydropyrimidin-4-yl)methyl)morpholin-2-yl)acetic acidHCID 11810751953.3%

Reaction Steps

Ethyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(1-(2-ethoxy-2-oxoethyl)-1H-1,2,4-triazol-3-yl)-1,4-dihydropyrimidine-5-carboxylate (0.57 g, 1 mmol) was reacted with 2-(morpholin-2-yl)acetic acid hydrochloride (0.3 g, 1.65 mmol) according to the procedure as described in Example 1, Step C to give the title compound as a yellow solid (0.34 g, 53%). 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-e62762c6edf049f6b0fcf4492c5b7d78
Source noteuspto-grants-2016_05