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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080186Generated: November 1, 2026

1-Hydroxybenzotriazole → 2,6-Diamino-N-(5-benzyl-thiophen-2-ylmethyl)-nicotinamide

https://huagongshe.com/reaction/2080186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2,6-Diaminonicotinic acidHCID 18977245—
Reactant2-Thiophenemethanamine,5-(phenylmethyl)-HCID 23130612—
SolventDimethyl SulfoxideHCID 679—
SolventSodium chloride; waterHCID 57417360—
Product2,6-Diamino-N-(5-benzyl-thiophen-2-ylmethyl)-nicotinamideHCID 2313035830%

Reaction Steps

To a solution of 2,6-diaminonicotinic acid described in Preparation Example A-15 (173 mg, 1.13 mmol) in dimethylsulfoxide (15 mL) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (433 mg, 2.26 mmol), 1-hydroxybenzotriazole (346 mg, 2.26 mmol) and C-(5-benzyl-thiophen-2-yl)-methylamine described in Preparation Example 42 (230 mg, 1.13 mmol), and the solution was stirred at room temperature fro 16 hours 30 minutes. The reaction solution was poured into brine, the solution was extracted with ethyl acetate, the organic layer was dried over anhydrous magnesium sulfate and then concentrated. The obtained residue was subjected to NH silica gel column chromatography, eluted with solvent (ethyl acetate) and the title compound (114 mg, 0.34 mmol, 30%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-66fafe050d8140739905096af590ecdc
Source noteuspto-grants-2011_04