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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232206Generated: October 27, 2026

Acetic Acid → 1-amino-2,3-dihydro-7-hydroxy-4-methyl-6-piperidinylacetylaminomethyl-1H-indene dihydrochloride

https://huagongshe.com/reaction/2232206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant(2,3-dihydro-7-hydroxy-1-hydroxy-imino-4-methyl-1H-indene-6-yl)methylaminocarbonylmethylpyridinium chlorideHCID 131715782—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventDiethyl ether ethanolHCID 21585056—
Product1-amino-2,3-dihydro-7-hydroxy-4-methyl-6-piperidinylacetylaminomethyl-1H-indene dihydrochlorideHCID 67882703—

Reaction Steps

10 Grams of (2,3-dihydro-7-hydroxy-1-hydroxy-imino-4-methyl-1H-indene-6-yl)methylaminocarbonylmethylpyridinium chloride, 200 ml of acetic acid and 1.0 g of platinum oxide were subjected to catalytic hydrogenation under 3 atmospheric hydrogen gas pressure at room temperature for 8 hours. After the hydrogenation was completed, the catalyst was removed by filtration, and the filtrate was concentrated to dryness under a reduced pressure. The residue thus obtained was dissolved in 100 ml of methanol and under ice-cooled condition, a methanol solution saturated with hydrogen chloride gas was added thereto so as to adjust the pH of the solution to about pH 1, then the said solution was concentrated to dryness under a reduced pressure. The residue thus obtained was recrystallzed from ethanol-diethyl ether to obtain 4.8 g of 1-amino-2,3-dihydro-7-hydroxy-4-methyl-6-piperidinylacetylaminomethyl-1H-indene dihydrochloride. Colorless powdery crystals. Melting point: 146° C. (decomposed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788130
Source datasetuspto-grants-1988_11
ORD IDord-5b645df872ac4cb7b6339549252ea6ce
Source noteuspto-grants-1988_11