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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881935Generated: November 1, 2026

1-Hydroxybenzotriazole → HCID 59331371, compound

https://huagongshe.com/reaction/1881935

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—
ReactantHCID 59331529HCID 59331529—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 59331371HCID 59331371639.3%

Reaction Steps

A solution of N-methoxymethanamine hydrochloride (662 mg) in acetonitrile (23 mL) was neutralized with triethylamine (2.34 mL), and 2-[4-(methylsulfonyl)phenyl]-3-(tetrahydrofuran-3-yl)propanoic acid (1.69 g), N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (1.30 g) and 1-hydroxybenzotriazole (104 mg) were added under ice-cooling. The reaction mixture was stirred overnight at room temperature, diluted with ethyl acetate, and washed with water 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 (1.68 g, yield 87%) was obtained as a colorless amorphous solid from a fraction eluted with ethyl acetate-hexane (99:1, volume ratio).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-ca634ff3dbcb4e588d2b60ed3ef73f09
Source noteuspto-grants-2012_11