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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650081Generated: October 31, 2026

Ammonia → HCID 136365320, compound

https://huagongshe.com/reaction/650081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantGuanidine HydrochlorideHCID 5742—
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 21714298HCID 21714298—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventDimethylformamideHCID 6228—
ProductHCID 136365320HCID 136365320—

Reaction Conditions

Temperature67.5 °C

Reaction Steps

Crude N-(aminoiminomethyl)-5,6,7,8-tetrahydro-11-chloro-10-methoxymethyloxy-8-oxo-4H-azocino[3,2,1-hi]indole-2-carboxamide was obtained by carrying out reaction according to the method described in Example 1, except for using ethyl 5,6,7,8-tetrahydro-11-chloro-10-methoxymethyloxy-8-oxo-4H-azocino[3,2,1-hi]indole-2-carboxylate (0.50 g, 1.36 mmol), guanidine hydrochloride (2.60 g, 27.2 mmol), sodium methoxide (1.47 g, 27.2 mmol) and N,N-dimethylformamide (50 ml). Subsequently, the crude product was added to a mixture of isopropanol (70 ml), water (20 ml) and methanesulfonic acid (0.50 g), and the resulting mixture was stirred at 65-70° C. for 6 hours. The reaction mixture was neutralized with 28% aqueous ammonia and extracted three times with ethyl acetate, and the extract solution was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was dissolved in tetrahydrofuran (70 ml), after which methanesulfonic acid (0.26 g) was added and the solid precipitated was collected by filtration. The solid collected was recrystallized from a mixture of isopropanol (1 ml) and water (20 ml) to obtain 0.25 g of N-(aminoiminomethyl)-5,6,7,8-tetrahydro-11-chloro-10-hydroxy-8-oxo-4H-azocino[3,2,1-hi]indole-2-carboxamide methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271251B1
Source datasetuspto-grants-2001_08
ORD IDord-d4e66b730b9a41c5b57bbc411270830f
Source noteuspto-grants-2001_08