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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174518Generated: October 31, 2026

Diisopropylcarbodiimide → 1-(4-Methoxynaphthalene-1-sulfonyl)-2,3-dihydro-1H-indole-3-carboxylic Acid [2-(1-methyl-pyrrolidin-2-yl)-ethyl]amide

https://huagongshe.com/reaction/1174518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-(2-Aminoethyl)-1-methylpyrrolidineHCID 98388—
Reactant1-(4-methoxynaphthalene-1-sulfonyl)-2,3-dihydro-1H-indole-3-carboxylic AcidHCID 68769872—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(4-Methoxynaphthalene-1-sulfonyl)-2,3-dihydro-1H-indole-3-carboxylic Acid [2-(1-methyl-pyrrolidin-2-yl)-ethyl]amideHCID 987034269%

Reaction Steps

To a solution of 1-(4-methoxynaphthalene-1-sulfonyl)-2,3-dihydro-1H-indole-3-carboxylic acid (C) (900 mg, 2.35 mmol) in dichloromethane (20 cm3) was added 1-hydroxybenzotriazole (HOBT, 0.48 g, 3.53 mmol) and 1,3-diisopropylcarbodidiimide (DIC, 0.55 cm3, 3.53 mmol). This was left to stir at room temperature for 5 min, before adding 2-(1-methyl-pyrrolidin-2-yl)-ethylamine (0.342 cm3, 2.35 mmol). The reaction was stirred for 16 h at room temperature before water (60 cm3) was added followed by dichloromethane (60 cm3). The resulting mixture was then shaken and the organic layer was washed with water (40 cm3), saturated aqueous sodium bicarbonate solution (40 cm3), water again (40 cm3) and then saturated aqueous sodium chloride solution (50 cm3) before the organic portion was dried over sodium sulfate, It was then evaporated under reduced pressure to afford the title compound (1) (800 mg, 1.62 mmol, 69%), positive ion ESI (M+H)+ 494.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838518B2
Source datasetuspto-grants-2010_11
ORD IDord-4ef310abf07b47d4a52042046521f4af
Source noteuspto-grants-2010_11