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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855433Generated: October 28, 2026

4-tert-Butylbenzaldehyde → HCID 86603117, compound

https://huagongshe.com/reaction/855433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzaldehydeHCID 70324—
Reactant1H-Indole-7-carboxylic acidHCID 74281—
Reactant4-PyridineethanamineHCID 83275—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 86603117HCID 8660311758.3%

Reaction Steps

81 mg (0.5 mmol) of 4-tert-butyl benzaldehyde and 61 mg (0.5 mmol) of 2-(4-pyridyl)-ethyl amine were dissolved in 2 ml methanol and the solution was stirred for 2 h at rt. 18.5 mg (0.5 mmol) of sodium borohydride were added in portions under nitrogen. The reaction mixture was stirred at rt for 30 min, the solvent was evaporated and the residue was suspended in 4 ml DCM. 88 mg (0.55 mol) of 1H-indole-7-carboxylic acid and 105 mg (0.55 mmol) of EDC.HCl were added and the mixture was stirred at rt over night. The product was purified by column chromatography (silica gel; diethyl ether) to yield 120 mg (58%) product as a colorless oil. MS (ISP) 412.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-51dd32b747a44534b712392a71598713
Source noteuspto-grants-2007_08