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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077528Generated: October 30, 2026

Potassium Carbonate → N-(6-(5-amino-6-methylpyridin-3-yl)benzo[d]thiazol-2-yl)acetamide

https://huagongshe.com/reaction/2077528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-methylpyridin-3-amineHCID 21964096—
Reactantn-(6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazol-2-yl)acetamideHCID 51354026—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductN-(6-(5-amino-6-methylpyridin-3-yl)benzo[d]thiazol-2-yl)acetamideHCID 5135459850.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-bromo-2-methylpyridin-3-amine (224.9 mg, 1.202 mmol), N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazol-2-yl)acetamide (413.7 mg, 1.300 mmol), potassium carbonate (549.4 mg, 3.975 mmol), and Pd(dppf)Cl2*DCM complex (108.7 mg, 0.133 mmol) were suspended in DME (5.0 ml) and water (1.25 ml), and the flask was fit with a reflux condensor and argon was bubbled through for about 15 seconds. Then, the flask was placed in a preheated oil bath (100° C.) and stirred under argon for 80 minutes. The reaction was cooled to room temperature, and the aqueous phase was removed via pipette. The reaction was then concentrated, treated with MeOH, and filtered. Solid washed with MeOH, water, MeOH, and Et2O. Solid then collected and dried under high vacuum to afford N-(6-(5-amino-6-methylpyridin-3-yl)benzo[d]thiazol-2-yl)acetamide (179.7 mg, 50% yield). MS (ESI pos. ion) m/z: 299. Calculated exact mass for C15H14N4OS: 298.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928140B2
Source datasetuspto-grants-2011_04
ORD IDord-dd4eeb1b724c41539a6e317fa3bd4ac8
Source noteuspto-grants-2011_04