HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393578Generated: October 26, 2026
Tris(hydroxymethyl)aminomethane → 7-methyl-2-Quinolinecarboxamide
https://huagongshe.com/reaction/393578
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | (9H-Fluoren-9-yl)methyl 2-oxoethylcarbamate | HCID 10858926 | — |
| Reactant | 7-Methylquinoline-2-carboxylic acid | HCID 21919328 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-methyl-2-Quinolinecarboxamide | HCID 23532041 | 339.2% |
Reaction Steps
A solution of the amine 4 (1.0 mg, 1.9 μmol, 1.0 equiv) in dichloromethane (0.1 mL) was added to 7-methylquinoline-2-carboxylic acid (2.8 μmol, 1.5 equiv) and 1-hydroxybenzotriazole (0.44 mg, 3.2 μmol, 1.7 equiv) in a vial at 23° C. The solution was stirred for 5 min, then N-cyclohexylcarbodiimide-N′-propyloxymethyl polystyrene (Argonaut Technologies, 1.13 mmol/g, 3.4 mg, 3.8 μmol, 2.0 equiv) was added in one portion at 23° C. The reaction mixture was stirred gently at 23° C. under an argon atmosphere for 16 h. PS-Trisamine (Argonaut Technologies, 4.71 mmol/g, 2.0 mg, 9.5 μmol, 5.0 equiv) was then added in one portion and the reaction mixture was stirred for a further 2 h. The mixture was filtered through Celite (0.5 cm) and concentrated in vacuo to give the 7-methylquinoline-2-carboxylic acid amide derivative (1.2 mg, 95%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809099B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-82ab64e60a14437f9cff576b56e52ce1 |
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| Source note | uspto-grants-2004_10 |
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