HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079961Generated: October 31, 2026
Triethylamine → 6-amino-N-(5-benzylthiophen-2-ylmethyl)-nicotinamide
https://huagongshe.com/reaction/2079961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Aminonicotinic acid | HCID 18496 | — |
| Reactant | Benzotriazol-1-yltris(dimethylamino)phosphonium hexafluorophosphate | HCID 10938826 | — |
| Reactant | 2-Thiophenemethanamine,5-(phenylmethyl)- | HCID 23130612 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-amino-N-(5-benzylthiophen-2-ylmethyl)-nicotinamide | HCID 23130353 | 29.5% |
Reaction Steps
To a solution of 6-aminonicotinic acid (340 mg, 2.4 mmol) and C-(5-benzyl-thiophen-2-yl)-methylamine described in Preparation Example 42 (450 mg, 2.2 mmol) in N,N-dimethylformamide (5 mL) were added benzotriazol-1-yl-tris(dimethylamino)phosphonium hexafluorophosphate (1.1 g, 2.4 mmol) and triethylamine(0.62 mL, 4.4 mmol), and the solution was stirred at 60° C. for 1 hour. Water and ethyl acetate were added to the reaction solution, which was then partitioned, and the organic layer was washed twice with water. Silica gel was added to the organic layer, the solvent was evaporated in vacuo adsorption, purification was carried out by NH silica gel column chromatography (hexane:ethyl acetate=1:1, then ethyl acetate, then ethyl acetate:methanol=10:1), and 6-amino-N-(5-benzyl-thiophen-2-ylmethyl)-nicotinamide (210 mg, 0.65 mmol, 29.5%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932272B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-07255c3963894ecca90e46bbafeb493a |
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| Source note | uspto-grants-2011_04 |
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