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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056517Generated: October 25, 2026

Diisopropylethylamine → 2-(2-(6-(2,4-dimethoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)ethyl)guanidine

https://huagongshe.com/reaction/1056517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPyrazole-1-carboxamidine monohydrochlorideHCID 2734672—
Reactant1-(2-aminoethyl)-6-(2,4-dimethoxyphenyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one hydrochlorideHCID 86684680—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Product2-(2-(6-(2,4-dimethoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)ethyl)guanidineHCID 86684682—

Reaction Conditions

Temperature55 °C

Reaction Steps

Diisopropylethylamine (0.22 mL, 1.3 mmol) was added to a suspension of 1-(2-aminoethyl)-6-(2,4-dimethoxyphenyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one hydrochloride (181.6 mg, 0.528 mmol) (the product of Example 6) and 1H-pyrazole-1-carboxamidine hydrochloride (90.6 mg, 0.618 mmol) in DMF (0.55 mL). After heating for 1 h at 55° C., the reaction mixture was cooled to ambient temperature, diluted with EtOH (1.6 mL), and the solid product collected by vacuum filtration, rinsing with additional EtOH. The isolated solid was re-suspended in EtOH (2.1 mL) for 3 h at r.t. before being collected again by vacuum filtration and rinsing with additional EtOH. The desired product was obtained, after drying, as a colorless solid. Solubility data for this product is consistent with it being in its zwitterionic form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399626B2
Source datasetuspto-grants-2016_07
ORD IDord-557a2456f3b545a5a2527875a72f4977
Source noteuspto-grants-2016_07