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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393590Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 18976209, compound

https://huagongshe.com/reaction/2393590

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,2,3,4-Tetrahydro-2-naphthoic acidHCID 101370—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 18976150HCID 18976150—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 18976209HCID 1897620975.4%

Reaction Steps

Under ice cooling, 1.10 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride was added to a stirred mixture of 1.22 g of 3-amino-2,3-dihydro-1-pentyl-1H-indol-2-one hydrochloride, 0.93 g of 1,2,3,4-tetrahydronaphthalene-2-carboxylic acid, 0.72 g of 1-hydroxybenzotriazole and 40 ml of methylene chloride. After the reaction mixture was stirred under ice cooling for 1 hour, 1.0 ml of triethylamine was added to the mixture. The resulting mixture was stirred under ice cooling for 2 hours and then stirred at room temperature for 2 hours. The solvent was removed by evaporation under reduced pressure. The residue was extracted with ethyl acetate, and the extract was washed and dried. After removal of solvent, the residual solid was recrystallized from ethyl acetate-hexane to afford 1.36 g of N-(2,3-dihydro-2-oxo-1-pentyl-1H-indol-3-yl)-1,2,3,4-tetrahydronaphthalene-2-carboxamide as colorless crystals. Melting point: 127° to 132° C., IR (Nujol) (cm-1): 3280, 1725, 1640, 1610, MS (m/z): 376 (M+), 218 (base), 147, 31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807883
Source datasetuspto-grants-1998_09
ORD IDord-57c7ca4161c945328ec46f4abe9b3bf8
Source noteuspto-grants-1998_09