Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352173Generated: October 31, 2026

1,2-Ethanediamine, N1-phenyl- → HCID 17838262, compound

https://huagongshe.com/reaction/1352173

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Ethanediamine, N1-phenyl-HCID 74270—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(1H-5-Indazolylamino)-1-cyclohexanoneHCID 17838271—
ReactantHydrochloride methanolHCID 21893726—
SolventMethanolHCID 887—
ProductHCID 17838262HCID 1783826268.3%

Reaction Steps

4-(1H-5-Indazolylamino)-1-cyclohexanone (intermediate 3) (57 mg) and N-phenylethylenediamine (68 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] to give an anti-form compound (51 mg) and a syn-form compound (45 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217722B2
Source datasetuspto-grants-2007_05
ORD IDord-6cc5f863cc3a4bea896b4052341fe1f0
Source noteuspto-grants-2007_05