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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589476Generated: November 2, 2026

Pyridine → HCID 178492415, compound

https://huagongshe.com/reaction/1589476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 54016649HCID 54016649—
ReactantHCID 178479438HCID 178479438—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 178492415HCID 17849241577%

Reaction Steps

To 40 ml of anhydrous pyridine, was added 2.1 g of 6-guanidinocaproic acid hydrochloride. To the mixture, while being cooled in ice, was added 2.5 g of DCC. The mixture was stirred for one hour, admixed with 2.6 g of 4-amidino-2-methoxyphenol methanesulfonate, and further stirred overnight at room temperature. After addition of ethyl ether to the reaction mixture, the supernatant was removed to obtain an oily substance as the residue. The oily substance was dissolved in DMF, then freed from insolubles by filtration, and mixed with ethyl ether to obtain 4.0 g of a colorless oily substance. This substance was dissolved in water by heating, then treated with activated carbon, and mixed with acetone to isolate 3.5 g of 4-amidino-2-methoxyphenyl 6-guanidinocaproate methanesulfonate hydrochloride in the form of colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04570006
Source datasetuspto-grants-1986_02
ORD IDord-c74e1923c8bb4c4582e91495a4b1f2ac
Source noteuspto-grants-1986_02