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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871037Generated: October 30, 2026

Water → Tert-butyl 4-(4-aminoisothiazol-5-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/871037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium DithioniteHCID 24489—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 4-(4-nitroisothiazol-5-yloxy)piperidine-1-carboxylateHCID 86720856—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(4-aminoisothiazol-5-yloxy)piperidine-1-carboxylateHCID 8672085740.3%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a solution of tert-butyl 4-(4-nitroisothiazol-5-yloxy)piperidine-1-carboxylate (1C3) (213 mg, 0.67 mmol) in methanol (4 mL) at room temperature was added water (3 mL), saturated NaHCO3 solution (3 mL) and Na2S2O4 (340 mg, 2 mmol). The mixture was stirred at 35° C. for 3 hours, cooled to room temperature, diluted with ethyl acetate (100 mL), washed with brine, dried over Na2SO4, and concentrated in vacuo at room temperature (25° C.). The residue was purified with flash column (eluent: 10-30% ethyl acetate/petroleum ether) to afford the product tert-butyl 4-(4-aminoisothiazol-5-yloxy)piperidine-1-carboxylate (1D4) (80 mg, 0.27 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969584B2
Source datasetuspto-grants-2015_03
ORD IDord-ec200daa69da4d1da7b3e9fa9cf94aaa
Source noteuspto-grants-2015_03