HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911998Generated: October 26, 2026
Dimethyl Sulfide → N-(1-(3-(Methylthio)benzyl)piperidin-3-yl)-1H-indazol-5-amine
https://huagongshe.com/reaction/1911998
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | 2,2-Dimethyl-1-(5-(1-(3-(methylthio)benzoyl)piperidin-3-ylamino)-1H-indazol-1-yl)propan-1-one | HCID 59799774 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(1-(3-(Methylthio)benzyl)piperidin-3-yl)-1H-indazol-5-amine | HCID 57446046 | 41.1% |
Reaction Steps
Into a round bottom flask was added 2,2-dimethyl-1-(5-(1-(3-(methylthio)benzoyl)-piperidin-3-ylamino)-1H-indazol-1-yl)propan-1-one (240 mg, 0.655 mmol) and THF (3 mL). The solution was heated to 60° C. and borane-dimethyl sulfide complex in THF (3.0 mL of a 2.0M solution in THF, 6.0 mmol) was added, allowing dimethyl sulfide to distill off. After the starting material was consumed, the reaction was evaporated, 5N NaOH (10 mL) was added, and the mixture was extracted with EtOAc. The organic phases were dried, evaporated, and the residue was chromatographed on silica gel, eluting with 3/1-EtOAc/Heptane to afford the title compound (95 mg, 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604218B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-603a25ebee8847c4b3af4d9cd1cb6a09 |
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| Source note | uspto-grants-2013_12 |
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