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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352169Generated: November 1, 2026

Thiopheneethanamine → HCID 17838037, compound

https://huagongshe.com/reaction/1352169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneethanamineHCID 116521—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(1H-5-Indazolylamino)-1-cyclohexanoneHCID 17838271—
ReactantHydrochloride methanolHCID 21893726—
SolventMethanolHCID 887—
ProductHCID 17838037HCID 1783803731%

Reaction Steps

4-(1H-5-Indazolylamino)-1-cyclohexanone (intermediate 3) (57 mg) and 2-thiophenethylamine (64 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 (21 mg) and a syn-form compound (14 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217722B2
Source datasetuspto-grants-2007_05
ORD IDord-fb37f9ef3b0d465f978e92a66a371e8e
Source noteuspto-grants-2007_05