Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243031Generated: November 2, 2026

Water → Ethyl 2-[6-(3-ethyl-ureido)-pyridin-3-yl]-4-isopropylcarbamoyl-thiazole-5-carboxylate

https://huagongshe.com/reaction/2243031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant6-(3-Ethylureido)pyridine-3-boronic acid pinacol esterHCID 59208434—
ReactantEthyl 2-chloro-4-isopropylcarbamoyl-thiazole-5-carboxylateHCID 59208444—
CatalystHCID 178420553HCID 178420553—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-[6-(3-ethyl-ureido)-pyridin-3-yl]-4-isopropylcarbamoyl-thiazole-5-carboxylateHCID 5920840417.72%

Reaction Conditions

Temperature100 °C

Reaction Steps

In a 10 mL of microwave vial, ethyl 2-chloro-4-isopropylcarbamoyl-thiazole-5-carboxylate (Intermediate 28, 1.1 g, 3.97 mmol), N-ethyl-N′-[5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridin-2-yl]-urea (Intermediate 1, 1.15 g, 3.97 mmol), cesium carbonate (1.29 g, 3.97 mmol), Tetrakis (triphenylphosphino) palladium (0) (0.458 g, 0.397 mmol) in 15 mL of 4:1 dioxane:H2O was degassed for 30 min, then heated to 100° C. for 30 min. The reaction mixture was diluted with ethyl acetate (25 mL), then washed with water (10 mL). The organic layer was dried, then concentrated under reduced pressure to yield crude a residue which was purified by column chromatography over silica gel to afford 0.195 g (17.72%) of the title compound as solid. MS (APCI): 406 (M+H−) for C18H23N5O4S; NMR: 1.13 (t, 3H), δ 1.16 (d, 6H), 1.28 (t, 3H), δ 3.2 (q, 2H), 4.04 (m, 1H), 4.29 (q, 2H), 7.63 (d, 1H), 7.70 (br s, 1H), 8.27 (dd, 1H), δ 8.45 (d, 1H), 8.83 (d, 1H), 9.56 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674801B2
Source datasetuspto-grants-2010_03
ORD IDord-01f73cd47cc241c68edf6585b3082a5e
Source noteuspto-grants-2010_03