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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517521Generated: October 31, 2026

Acetic Acid → HCID 25154364, compound

https://huagongshe.com/reaction/1517521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylamineHCID 674—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 58173147HCID 58173147—
SolventMethanolHCID 887—
ProductHCID 25154364HCID 25154364—

Reaction Steps

(Method 2): 6-(1,3,5-Trimethyl-1H-pyrazol-4-yl)-indan-1-one (1.1 mmol) was dissolved in MeOH. Dimethyl-amine (24.5 mmol), acetic acid (0.11 mmol) and sodium cyanoborohydride (2.2 mmol) were added under argon atmosphere. The suspension was refluxed overnight and then cooled. The crude was evaporated to dryness and then suspended in water. The product was extracted with CH2Cl2 and washed with water. The CH2Cl2 extract was dried with anhydrous Na2SO4, filtered and evaporated to dryness to give the crude product dimethyl-[6-(1,3,5-trimethyl-1H-pyrazol-4-yl)-indan-1-yl]-amine. The crude was purified by flash column chromatography (CH2Cl2-MeOH as eluents) by using a CombiFlash Companion™ system to yield the base of the title compound. The obtained product was diluted in ethyl acetate and a solution of hydrogen chloride 2.0 M in diethylether was added. The resulting precipitate was filtered and dried under vacuum to yield the title compound dimethyl-[6-(1,3,5-trimethyl-1H-pyrazol-4-yl)-indan-1-yl]-amine dihydrochloride (79%). MS [MH]+=270.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232307B2
Source datasetuspto-grants-2012_07
ORD IDord-0e5210ea7e504740ac12b7c747e3b57a
Source noteuspto-grants-2012_07