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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782146Generated: November 3, 2026

HCID 54757412, compound → HCID 54757413, compound

https://huagongshe.com/reaction/1782146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54757412HCID 54757412—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 54757413HCID 54757413—

Reaction Steps

To a solution of 6-(1-azido-2-methyl-propyl)-5-benzyl-3-methyl-5H-isothiazolo[5,4-d]pyramidin-4-one (method 29) (0.5 g, 1.41 mmol) in methanol (20 mL) was added 5% Pd/C (20% by wt.) and the resulting mixture was stirred at r.t. in an atmosphere of H2 and the progress of the reaction was monitored by MS. After the disappearance of the starting material the reaction mixture was filtered through celite and washed with EtOAc. Concentration of the filtrate provided 6-(1-amino-2-methyl-propyl)-5-benzyl-3-methyl-5H-isothiazolo[5,4-d]pyrimidin-4-one as a thick oil. The product was used as such in the next reaction with out further purification. m/z 349 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498333B2
Source datasetuspto-grants-2009_03
ORD IDord-e3cec36b897f4f80a2ba67d2862cffbe
Source noteuspto-grants-2009_03