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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429586Generated: October 31, 2026

Potassium Carbonate → tert-butyl 4-(2-(piperidin-4-yloxy)benzo[d]thiazol-6-yl)-5,6-dihydropyridine-1(2H)-carboxylate

https://huagongshe.com/reaction/1429586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 4642098—
Reactant6-Bromo-2-(piperidin-4-yloxy)-benzothiazoleHCID 67466824—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl 4-(2-(piperidin-4-yloxy)benzo[d]thiazol-6-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 6746842587%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a degassed mixture of 6-bromo-2-(piperidin-4-yloxy)benzo[d]thiazole (Compound 1B, 400 mg, 1.277 mmol), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate (987 mg, 3.19 mmol) and K2CO3 (706 mg, 5.11 mmol) in dioxane (20 mL) and water (6.67 mL) was added Pd(PPh3)4 (148 mg, 0.128 mmol) and the resulting mixture was heated at 95° C. for 3.5 h. The mixture was cooled to room temperature, diluted with water (15 mL), and extracted with EtOAc (3×10 mL). The combined organic layers were washed with brine, dried (Na2SO4), and evaporated. The crude product was purified by column chromatography (silica gel, CH2Cl2-MeOH gradient 0 to 15% MeOH) to afford Compound 50A (460.7 mg, 1.109 mmol, 87% yield) as a light yellow solid. LCMS (m/z)=416 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940716B2
Source datasetuspto-grants-2015_01
ORD IDord-38e3408fca9d4153b1e1ec95e62873c1
Source noteuspto-grants-2015_01