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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910965Generated: October 31, 2026

Potassium Carbonate → tert-Butyl 2-(3-(2-(4-methylthiazol-2-ylamino)pyridin-4-ylthio)phenoxy)acetate

https://huagongshe.com/reaction/910965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant3-(2-(4-Methylthiazol-2-ylamino)pyridin-4-ylthio)phenolHCID 57898930—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 2-(3-(2-(4-methylthiazol-2-ylamino)pyridin-4-ylthio)phenoxy)acetateHCID 2482642660%

Reaction Steps

A mixture of potassium carbonate (1.08 g, 7.82 mmol), 3-(2-(4-methylthiazol-2-ylamino)pyridin-4-ylthio)phenol (0.274 g, 0.869 mmol), and tert-butyl 2-bromoacetate (0.169 g, 0.869 mmol) in DMF (5 mL). The reaction mixture was stirred at room temperature overnight, then diluted with water and extracted with ethyl acetate. The combined organic layers were dried over magnesium sulfate, filtered and concentrated. The residue was purified using prepacked silica gel column chromatography with 15-20% ethyl acetate to afford the desired product (0.224 g, 58.8% yield) as light yellow solid. 1H NMR (CDCl3) δ 8.08 (d, 1H), 7.33 (t, 1H), 7.15 (m, 1H), 7.04 (t, 1H), 6.98 (m, 1H), 6.57 (dd, 1H), 6.49 (dd, 1H), 6.33 (d, 1H), 4.50 (s, 2H, 2.22 (d, 3H), 1.46 (s, 9H); Mass spectrum (esi) m/z=430 (100)(M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022222B2
Source datasetuspto-grants-2011_09
ORD IDord-3189a4eb91754b03a211f6874cb80d0c
Source noteuspto-grants-2011_09