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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787778Generated: October 30, 2026

Triethylamine → N-(5-amino-6-oxo-3-pentyl-2-thioxo-1,2,3,6-tetrahydropyrimidin-4-yl)cyclobutanecarboxamide

https://huagongshe.com/reaction/1787778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclobutanecarboxylic acidHCID 19494—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant5,6-Diamino-1-pentyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-oneHCID 57600254—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(5-amino-6-oxo-3-pentyl-2-thioxo-1,2,3,6-tetrahydropyrimidin-4-yl)cyclobutanecarboxamideHCID 5760017483.3%

Reaction Steps

The mixture of 5,6-diamino-1-pentyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one (1060 mg, 0.00464 mol), cyclobutane carboxylic acid (0.55 g, 5.5 mmol), benzotriazol-1-yloxytris (dimethylamino)phosphonium hexafluorophosphate (2.2 g, 5.1 mmol) and triethylamine (1.3 mL, 9.3 mmol) in DMF (20 mL) was stirred at room temperature for 4 hours. The mixture was diluted with water. The precipitate formed was filtered and dried to yield the desired product (1.20 g, 83.27%). LCMS calculated for C14H23N4O2S(M+H): 311.2; found 311.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511050B2
Source datasetuspto-grants-2009_03
ORD IDord-18959035390142b08c14f23249d9e933
Source noteuspto-grants-2009_03