HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167763Generated: November 2, 2026
6-Chloronicotinic acid → HCID 22993400, compound
https://huagongshe.com/reaction/1167763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Chloronicotinic acid | HCID 79222 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 4-Methoxy-7-morpholinobenzo[d]thiazol-2-amine | HCID 11402861 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22993400 | HCID 22993400 | 99.3% |
Reaction Steps
To a stirred solution of 1.89 g (7.54 mmol) 6-chloro-nicotinic acid in 20 ml THF were added 2.87 g (7.54 mmol) HATU and 1.28 ml (7.54 mmol) N-ethyldiisopropylamine and stirring continued at room temperature for 30 minutes. A solution of 2.00 g (7.54 mmol) 4-methoxy-7-morpholin-4-yl-benzothiazol-2-ylamine in 20 ml dioxane and 4 ml DMF was then added and stirring continued at room temperature for 16 h. The reaction mixture was then poured into 350 ml water and the mixture stirred for 30 min. The resulting crystals were collected by filtration, washed with methanol and then with ether, and dried in vacuo to afford 3.03 g (99%) 6-chloro-N-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-nicotinamide as a yellow crystalline solid. ES-MS m/e (%): 429 (M{37Cl}+Na+, 15), 427 (M{35Cl}+Na+, 38). 407 (M{37Cl}+H+, 40), 405 (M{31Cl}+H+, 100)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620811B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-1afa525989e94031b6b2ba047e083cb0 |
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| Source note | uspto-grants-2003_09 |
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