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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080215Generated: November 1, 2026

Triethylamine → 6-Amino-N-(5-(2-cyclopropylvinyl)thiophen-2-ylmethyl)nicotinamide

https://huagongshe.com/reaction/2080215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant6-Aminonicotinic acidHCID 18496—
ReactantBenzotriazol-1-yltris(dimethylamino)phosphonium hexafluorophosphateHCID 10938826—
ReactantC-(5-(2-Cyclopropylvinyl)thiophen-2-yl)methylamineHCID 67119557—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-Amino-N-(5-(2-cyclopropylvinyl)thiophen-2-ylmethyl)nicotinamideHCID 6711963566.6%

Reaction Steps

6-Aminonicotinic acid (35 mg, 0.251 mmol), C-(5-(2-cyclopropylvinyl)thiophen-2-yl)methylamine described in Preparation Example 151 (45 mg, 0.251 mmol), benzotriazol-1-yl-tris(dimethylamino)phosphonium hexafluorophosphate (133 mg, 0.301 mmol) and triethylamine (0.042 mL, 0.301 mmol) were dissolved in N,N-dimethylformamide (3 mL), and the solution was stirred at room temperature for 3 hours. Water (10 mL) was added to the reaction solution, which was then extracted with ethyl acetate (30 mL). The organic layer was washed, dried over anhydrous magnesium sulfate, then, the solvent was evaporated in vacuo, the obtained residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=3:1), and the title compound (50 mg, 0.167 mmol, 66.6%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-7e48cadb1bcd4b22951a1201446d9ef8
Source noteuspto-grants-2011_04