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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167763Generated: November 2, 2026

6-Chloronicotinic acid → HCID 22993400, compound

https://huagongshe.com/reaction/1167763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloronicotinic acidHCID 79222—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant4-Methoxy-7-morpholinobenzo[d]thiazol-2-amineHCID 11402861—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22993400HCID 2299340099.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620811B2
Source datasetuspto-grants-2003_09
ORD IDord-1afa525989e94031b6b2ba047e083cb0
Source noteuspto-grants-2003_09