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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352162Generated: October 30, 2026

2-Butanamine, 3,3-dimethyl- → HCID 17838283, compound

https://huagongshe.com/reaction/1352162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butanamine, 3,3-dimethyl-HCID 520907—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(1H-5-Indazolylamino)-1-cyclohexanoneHCID 17838271—
ReactantHydrochloride methanolHCID 21893726—
SolventMethanolHCID 887—
ProductHCID 17838283HCID 1783828310.2%

Reaction Steps

4-(1H-5-Indazolylamino)-1-cyclohexanone (intermediate 3) (57 mg) and (2-amino-3,3-dimethylbutane (51 mg) were dissolved in methanol (1 ml), and sodium triacetoxyborohydride (105 mg) was added by portions to the solution at room temperature. The reaction mixture was stirred at room temperature for 18 hr. Hydrochloric acid-methanol was then added thereto, and the reaction mixture was stirred and was then concentrated. The residue was purified by HPLC [0.5% aqueous trifluoroacetic acid solution/acetonitrile]. A saturated aqueous sodium hydrogencarbonate solution (2 ml) was added to fractions containing respective compounds, followed by extraction with chloroform-propanol (3/1). The organic layers were dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure to give an anti-form compound (8 mg) and a syn-form compound (5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217722B2
Source datasetuspto-grants-2007_05
ORD IDord-5ee100871e244513a03c22f10a291245
Source noteuspto-grants-2007_05