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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881812Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 59331592, compound

https://huagongshe.com/reaction/1881812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Cyclopentyl-2-(4-methanesulfonyl-phenyl)propionic acidHCID 12069489—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 59331592HCID 5933159289.1%

Reaction Steps

To a solution (80 mL) of N-methoxymethanamine hydrochloride (2.20 g) in N,N-dimethylformamide was added triethylamine (3.10 mL) for neutralization, and 3-cyclopentyl-2-[4-(methylsulfonyl)phenyl]propanoic acid (5.95 g), N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (5.80 g) and 1-hydroxybenzotriazole (4.10 g) were added under ice-cooling. The reaction mixture was warmed to room temperature and stirred overnight. The reaction mixture was diluted with ethyl acetate, and washed with water, 1N aqueous hydrochloric acid solution and saturated aqueous sodium hydrogen carbonate. The ethyl acetate layer was dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and the title compound (6.07 g, yield 89%) was obtained as colorless amorphous crystals from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). MS: 340 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-a05c6be0242343ae883f0b41aea24b33
Source noteuspto-grants-2012_11