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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851457Generated: November 2, 2026

1-Hydroxybenzotriazole → 7-(Benzyloxy)-N-[2-(tritylthio)ethyl]-1H-indole-2-carboxamide

https://huagongshe.com/reaction/1851457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant7-(benzyloxy)-1H-indole-2-carboxylic acidHCID 13242192—
Reactant2-(Tritylthio)ethylamine hydrochlorideHCID 18427267—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product7-(Benzyloxy)-N-[2-(tritylthio)ethyl]-1H-indole-2-carboxamideHCID 5790185394%

Reaction Steps

To a mixture of 7-(benzyloxy)-1H-indole-2-carboxylic acid (0.80 g), 2-(tritylthio)ethylamine hydrochloride (1.07 g), 1H-1,2,3-benzotriazol-1-ol (0.49 g), triethylamine (0.50 mL) and N,N-dimethylformamide (15 mL) was added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (0.69 g) at 0° C., and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography and the title compound (1.60 g, yield 94%) was obtained as colorless crystals from a fraction eluted with ethyl acetate-hexane (2:3, volume ratio). melting point 156-157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-930d49e7295b4ad5a843051256a1c91a
Source noteuspto-grants-2015_02