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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981450Generated: November 2, 2026

HCID 53945002, compound → HCID 178505338, compound

https://huagongshe.com/reaction/1981450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53945002HCID 53945002—
ReactantHCID 178479379HCID 178479379—
SolventPyridineHCID 1049—
ProductHCID 178505338HCID 178505338—

Reaction Steps

Into 300 ml of dried pyridine, were dissolved 7.0 g of 4-guanidinobenzoyl chloride hydrochloride and 7.4 g of 4-amidino-2-nitrophenol methanesulfonate. The solution was stirred overnight at room temperature. The precipitate which was formed was collected by filtration, suspended in methanol and filtered. The filtrate and 300 ml of ethyl ether were stirred to precipitate a colorless solid substance which was collected by filtration, dissolved in a small volume of methanol, and stirred together with a saturated sodium bicarbonate solution to precipitate the intended carbonate. The precipitated carbonate was collected by filtration, then air-dried, suspended in a small volume of methanol, admixed with methanesulfonic acid at room temperature. After 10 minutes, ethyl ether was added to the reaction mixture to precipitate crystals. The crystals were collected by filtration, washed thoroughly with ethyl ether to obtain 4-amidino-2-nitrophenyl 4-guanidinobenzoate dimethanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04514416
Source datasetuspto-grants-1985_04
ORD IDord-c2a8120a495847a68fc976830c4ebba8
Source noteuspto-grants-1985_04