HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804598Generated: October 31, 2026
Methanethioamide → Tert-butyl 4-(1,3-thiazol-4-yl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1804598
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanethioamide | HCID 3005587 | — |
| Reactant | tert-Butyl 4-(2-Bromoacetyl)piperidine-1-carboxylate | HCID 18187487 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 4-(1,3-thiazol-4-yl)piperidine-1-carboxylate | HCID 53485228 | 63% |
Reaction Steps
The title compound from Step B above (500 mg, 1.63 mmol) was combined with thioformamide (100 mg, 1.63 mmol) in 5 mL of THF, warmed to 60° C., and stirred overnight. The mixture was cooled to RT and diluted with ethyl acetate. The solution was then washed with water followed by brine. The organics were dried over magnesium sulfate, filtered and concentrated under vacuum. Purification via preparative TLC plates (3×1000 μM) eluting with 60% ethyl acetate/hexane afforded the title compound (282 mg, 63%) as a clear oil. ESI-MS calculated for C13H20N2O2S: Exact Mass: 268.12. Found: 169.12 (M-Boc)+ and 291.14 (MNa)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354403B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-ea6c954d703d44fea793abfa1aa76855 |
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| Source note | uspto-grants-2013_01 |
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