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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680019Generated: November 1, 2026

HCID 86737764, compound → HCID 86737766, compound

https://huagongshe.com/reaction/1680019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86737764HCID 86737764—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 86737766HCID 8673776683%

Reaction Steps

A solution of 2.5 g (0.00354 mole) of benzyl 6-amino-1'-methyl-spiro[penam-2,4'-piperidine]-3-carboxylate di-p-toluenesulfonate (obtained in 8.1) in 1.5 liter of ethanol is subjected to hydrogenolysis in a Parr's apparatus under 3.2 kg/cm2 of hydrogen in the presence of 2 g of palladium on carbon (10% Pd). After 90 minutes, the reaction mixture is filtered and the filtrate is evaporated to dryness and lyophilized in 600 ml of water. 1.8 g of 6-amino-1'-methyl-spiro[penam-2,4'-piperidine]-3-carboxylic acid di-p-toluenesulfonate is obtained; yield: 83%; M.P. approx 155°-160° C. (start of decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04271172
Source datasetuspto-grants-1981_06
ORD IDord-7ba6bfc2bfb74a938598d378f8421aa3
Source noteuspto-grants-1981_06