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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847321Generated: October 29, 2026

Pyridinium chloride → HCID 178448275, compound

https://huagongshe.com/reaction/847321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridinium chlorideHCID 10176127—
ReactantHCID 178448276HCID 178448276—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178448275HCID 17844827576.4%

Reaction Steps

0.110 g (0.132 mmol) of benzyl [N-[(3S,5S,6S)-6-[[N-[N-(t-butoxycarbonyl)-3-phenyl-L-alanyl]-L-histidyl]amino]-7-cyclohexyl-5-hydroxy-3-isopropylheptyl]amidino]carbamate and 0.015 mg (0.132 mmol) of pyridine hydrochloride are dissolved in 2.4 ml of methanol and hydrogenated in the presence of 20 mg of palladium on charcoal (5%) for 3 hours at room temperature and atmospheric pressure. After completion of the hydrogen uptake the catalyst is filtered off and the filtrate is evaporated under reduced pressure. In this manner there is obtained 0.074 g of t-butyl [(S)-α-[[(S)-1-[[(1S,2S,4S)-1-(cyclohexylmethyl)-6-guanidino-2-hydroxy-4-isopropylhexyl]carbamoyl]-2-imidazol-4-ylethyl]carbamoyl]phenethyl]carbamate hydrochloride as an amorphous solid, MS: 697 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05140011
Source datasetuspto-grants-1992_08
ORD IDord-15860730490c4e02acc13c2bc434725c
Source noteuspto-grants-1992_08