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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352170Generated: October 25, 2026

Isobutylamine → N1-(1H-5-Indazolyl)-N4-isobutyl-1,4-cyclohexanediamine

https://huagongshe.com/reaction/1352170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(1H-5-Indazolylamino)-1-cyclohexanoneHCID 17838271—
ReactantHydrochloride methanolHCID 21893726—
SolventMethanolHCID 887—
ProductN1-(1H-5-Indazolyl)-N4-isobutyl-1,4-cyclohexanediamineHCID 1783811911.2%

Reaction Steps

4-(1H-5-Indazolylamino)-1-cyclohexanone (intermediate 3) (57 mg) and isobutylamine (37 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 (8 mg) and a syn-form compound (6 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217722B2
Source datasetuspto-grants-2007_05
ORD IDord-b5c4f08c936746c38f6b5276c2bd6094
Source noteuspto-grants-2007_05