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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352157Generated: October 31, 2026

Cyclopropanemethanamine → HCID 17838236, compound

https://huagongshe.com/reaction/1352157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanemethanamineHCID 75646—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(1H-5-Indazolylamino)-1-cyclohexanoneHCID 17838271—
ReactantHydrochloride methanolHCID 21893726—
SolventMethanolHCID 887—
ProductHCID 17838236HCID 1783823618.4%

Reaction Steps

4-(1H-5-Indazolylamino)-1-cyclohexanone (intermediate 3) (57 mg) and cyclopropylmethylamine (54 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 then 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 (13 mg) and a syn-form compound (7 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217722B2
Source datasetuspto-grants-2007_05
ORD IDord-044b73c4c0104403a349a908e1fe49e0
Source noteuspto-grants-2007_05