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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378122Generated: November 3, 2026

Piperidine → HCID 54188178, compound

https://huagongshe.com/reaction/1378122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 54112781HCID 54112781—
SolventDimethylformamideHCID 6228—
ProductHCID 54188178HCID 5418817882.2%

Reaction Steps

0.34 ml (3.45 mmol) of piperidine was added to a suspension of 400 mg (1.15 mmol) of (S)-1-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-11,11a-dihydro-8H, 10H-azeto[1,2-a]-imidazo[5,1-c]thieno[3,2-e][1,4]diazepin-8-one in 10 ml of N,N-dimethylformamide and the mixture was stirred at room temperature for 12 hours. The solution was evaporated and the residue was partitioned between methylene chloride and 2N sodium carbonate solution. The aqueous solution was extracted with methylene chloride and the organic phases were dried, filtered and evaporated. The residue was chromatographed (silica gel, methyl acetate/methanol 15:1). There were obtained 375 mg (82%) of (S)-1-(5-piperidin-1-ylmethyl-1,2,4-oxadiazol-3-yl)-11,11a-dihydro-8H, 10H-azeto[1,2-a]imidazo[5,1-c]thieno[3,2-e]-[1,4]diazepin-8-one as a colourless foam, Rf=0.22 (silica gel, methyl acetate/methanol 15:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-43b8e022933b419aa7dec9bf34c9f52b
Source noteuspto-grants-1997_09