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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272554Generated: November 3, 2026

Sodium Hydroxide → HCID 68452330, compound

https://huagongshe.com/reaction/272554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 5-amino-1H-indole-2-carboxylateHCID 10726872—
Reactant4789-07-5HCID 12364385—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 68452330HCID 6845233076.1%

Reaction Steps

A mixture of 0.204 g (1 mmol) 5-amino-1H-indole-2-carboxylic acid ethyl ester, 133 mg (1 mmol) 1-ethyl piperidone and 0.35 ml (1 mmol) titanium(IV)isopropoxide in 1 ml methanol was treated after 3 h at room temperature with 0.023 g (1 mmol) sodium borohydride and the mixture was allowed to react during 16 h at room temperature. The mixture was poured on 50 ml ice/water and treated with 50 ml ethyl acetate and 5 ml 1 N NaOH aq. After 20 min the mixture was filtered through decalite and the aqueous phase was extracted with 50 ml ethyl acetate. The combined organic phases were washed with 50 ml NaCl sat., dried over Na2SO4 and after filtration evaporated to dryness. The residue was purified over silica eluting with a gradient of dichloromethane (DCM)/2N NH3 in methanol and 0.240 g (76%) of the title compound were isolated as brown solid. MS (m/e): 316.1 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456174B2
Source datasetuspto-grants-2008_11
ORD IDord-86d65a8929044c65a1b30eec758d6811
Source noteuspto-grants-2008_11