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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-butyl 4-(4-nitroisothiazol-5-yloxy)piperidine-1-carboxylate | HCID 86720856 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 4-(4-aminoisothiazol-5-yloxy)piperidine-1-carboxylate | HCID 86720857 | 40.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969584B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-ec200daa69da4d1da7b3e9fa9cf94aaa |
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| Source note | uspto-grants-2015_03 |
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