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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097976Generated: October 30, 2026

Cyclopropanecarboximidamide hydrochloride → HCID 178490489, compound

https://huagongshe.com/reaction/2097976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboximidamide hydrochlorideHCID 2781916—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 68754038HCID 68754038—
SolventEthanolHCID 702—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178490489HCID 178490489—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of N-(2-(hydrazinecarbonyl)thiophen-3-yl)-2-(4-methoxyphenyl)acetamide (101 mg, 0.30 mmol), cyclopropylcarbamidine hydrochloride (47 mg, 0.39 mmol) and sodium methoxide (39 mg, 0.72 mmol) in ethanol (3 mL) was stirred at 120° C. for 17 h. The mixture was diluted with brine and extracted with ethyl acetate. The organic phase was separated, dried (Na2SO4), filtered, concentrated under vacuum and purified by preparative HPLC to give N-(2-(3-cyclopropyl-1H-1,2,4-triazol-5-yl)thiophen-3-yl)-2-(4-methoxyphenyl)acetamide. Retention time (min)=5.578, method [7], MS (ESI) 354.43 (M+H); 1H NMR (300 MHz, CDCl3) δ 10.48 (s, 1H), 8.11 (d, J=5.6 Hz, 1H), 7.25-7.32 (m, 3H), 6.94 (d, J=8.8 Hz, 2H), 3.83 (s, 3H), 3.74 (s, 2H), 1.98-2.03 (m, 1H), 1.07-1.17 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450363B2
Source datasetuspto-grants-2013_05
ORD IDord-cf913879fb3e491086b03eb85840cab9
Source noteuspto-grants-2013_05