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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080209Generated: November 1, 2026

Methylamine → HCID 23130668, compound

https://huagongshe.com/reaction/2080209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantA-101HCID 188218—
Reactant2-aminochloro-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamideHCID 23130498—
SolventDimethyl SulfoxideHCID 679—
SolventDiisopropylethylamineHCID 81531—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 23130668HCID 2313066873%

Reaction Conditions

Temperature135 °C

Reaction Steps

2-Amino-6-chloro-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide described in Example A-101 (200 mg, 0.56 mmol) was dissolved in a mixture solution of dimethylsulfoxide (1 mL) and diisopropylethylamine (0.5 mL), methylamine (2M tetrahydrofuran solution) (2 mL, 4 mmol) was added thereto, followed by heating in a sealed tube for 14 hours (oil bath temperature: 135° C.). The reaction mixture was allowed to room temperature, poured into brine, and the solution was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, then concentrated, the obtained residue was purified by NH silica gel column chromatography (ethyl acetate:hexane=2:1), and the title compound (144 mg, 0.41 mmol, 73%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-e378b38b21154627b3aba8d9cb2e2248
Source noteuspto-grants-2011_04