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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589510Generated: November 1, 2026

HCID 53945002, compound → HCID 178505338, compound

https://huagongshe.com/reaction/1589510

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 was 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 numberUS04570006
Source datasetuspto-grants-1986_02
ORD IDord-c397ff80d58e426f8bba59e49190aa30
Source noteuspto-grants-1986_02