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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524911Generated: October 30, 2026

1,1-Dimethylethyl 1-thia-6-azaspiro[2.5]octane-6-carboxylate → tert-Butyl 4-mercapto-4-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/524911

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Dimethylethyl 1-thia-6-azaspiro[2.5]octane-6-carboxylateHCID 18187971—
Reactant1H-benzo[d][1,2,3]triazol-1-yl 2-amino-6-(cyanomethyl)pyrazolo[1,5-a]pyrimidine-3-carboxylateHCID 90199892—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-mercapto-4-methylpiperidine-1-carboxylateHCID 71629631—

Reaction Steps

To a solution of tert-butyl 1-thia-6-azaspiro[2.5]octane-6-carboxylate (430 mg, 1.875 mmol) in THF (5 mL) was added LiAlH4 (Lithium Ion (1)) (0.9375 mL of 2 M, 1.875 mmol) and the solution was stirred at room temperature for 1 h. The reaction was quenched by careful dropwise addition of water (2 ml), stirred for 10 mins before the reaction mixture was partitioned between water and EtOAc. The organic extract was washed with brine, dried (MgSO4) and concentrated to give tert-butyl 4-methyl-4-sulfanyl-piperidine-1-carboxylate as a colorless oil. (380 mg, 87%). MS (ES−) 231.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340546B2
Source datasetuspto-grants-2016_05
ORD IDord-65edc1348a874e629453bfd658f3a1ee
Source noteuspto-grants-2016_05