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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911890Generated: October 26, 2026

Dimethyl Sulfide → N-(1-(3-(Methylthio)benzyl)piperidin-3-yl)-1H-indazol-5-amine

https://huagongshe.com/reaction/1911890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
Reactant2,2-Dimethyl-1-(5-(1-(3-(methylthio)benzoyl)piperidin-3-ylamino)-1H-indazol-1-yl)propan-1-oneHCID 59799774—
SolventTetrahydrofuranHCID 8028—
ProductN-(1-(3-(Methylthio)benzyl)piperidin-3-yl)-1H-indazol-5-amineHCID 5744604641.1%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604205B2
Source datasetuspto-grants-2013_12
ORD IDord-05ac4bf381be4467977a4d8fc9396c99
Source noteuspto-grants-2013_12