HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079982Generated: October 30, 2026
Triethylamine → Quinoline-6-carboxylic acid cyanomethyl-amide
https://huagongshe.com/reaction/2079982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Quinolinecarboxylic acid | HCID 82571 | — |
| Reactant | Benzotriazol-1-yltris(dimethylamino)phosphonium hexafluorophosphate | HCID 10938826 | — |
| Reactant | Aminoacetonitrile hydrochloride | HCID 11491918 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Quinoline-6-carboxylic acid cyanomethyl-amide | HCID 58388078 | 69% |
Reaction Steps
To a solution of quinoline-6-carboxylic acid (500 mg, 2.9 mmol) and amino acetonitrile hydrochloride (320 mg, 3.4 mmol) in N,N-dimethylformamide (10 mL) were added benzotriazol-1-yl-tris(dimethylamino)phosphonium hexafluorophosphate (1.5 g, 3.48 mmol) and triethylamine (1.2 mL, 8.7 mmol), and the solution was stirred at 60° C. for 10 minutes. Ethyl acetate and water was added to the reaction solution, which was then partitioned, the organic layer was washed twice with water. Silica gel was added to the organic layer, the solvent was evaporated in vacuo for adsorption, purified by NH silica gel column chromatography (ethyl acetate), and the title compound (420 mg, 2.0 mmol, 68.9%) was obtained as a light brown solid.
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-03ffffbe175744569397c4bac26ba816 |
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| Source note | uspto-grants-2011_04 |
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