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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855437Generated: October 25, 2026

1H-Indole-7-carboxylic acid → 1H-Indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(ethyl-m-tolyl-amino)-ethyl]-amide

https://huagongshe.com/reaction/855437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indole-7-carboxylic acidHCID 74281—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN'-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamineHCID 69342865—
SolventDichloromethaneHCID 6344—
Product1H-Indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(ethyl-m-tolyl-amino)-ethyl]-amideHCID 8660312059.9%

Reaction Steps

81 mg (0.50 mol) of 1H-indole-7-carboxylic acid, 162 mg (0.5 mmol) of N′-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamine and 108 mg (0.55 mmol) of EDC.HCl were dissolved in 5 ml DCM. The reaction mixture was stirred at rt over night. The solvent was evaporated and the residue was dissolved in diethyl ether. The organic layer was washed with 1N aqueous HCl solution, once with 1N aqueous NaOH solution and once with saturated aqueous NaCl solution, dried over sodium sulfate, filtered and the solvent was evaporated to leave 140 mg (55%) product as a colorless oil. MS (ISP) 468.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-39ee5e229e144f9586dff008529c1e34
Source noteuspto-grants-2007_08