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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346493Generated: October 30, 2026

HCID 86595859, compound → HCID 86611452, compound

https://huagongshe.com/reaction/346493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86595859HCID 86595859—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 86611452HCID 86611452—

Reaction Steps

tert-Butyl [3-(1-cyanoethyl)-1,2,4-thiadiazol-5-yl]carbamate (0.65 mmol) was dissolved in MeOH (15 mL) and a catalytic amount of Raney-Ni (50% in H2O) was added. The reaction mixture was stirred at room temperature for 3 h under H2 (50 psi). The reaction mixture was filtered through a pad of CELITE and the solvent was removed under reduced pressure. Purification using preparative LCMS afforded the tert-butyl [3-(2-amino-1-methylethyl)-1,2,4-thiadiazol-5-yl]carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173030B2
Source datasetuspto-grants-2007_02
ORD IDord-cb6cf82429834e088681c112f5dcd456
Source noteuspto-grants-2007_02