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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486974Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 71493653, compound

https://huagongshe.com/reaction/1486974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantOxazol-5-yl-MethylaMine hydrochlorideHCID 45790095—
Reactant(Z)-3-(3-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,4-triazol-1-yl)acrylic acidHCID 86703006—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 71493653HCID 71493653—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 25 mL 3N round-bottomed flask equipped with nitrogen inlet, (Z)-3-(3-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,4-triazol-1-yl)acrylic acid (4) (0.250 g, 1.0 eq.) was dissolved in dichloromethane (5.0 mL, 20 V). The reaction mixture was cooled to 0° C. and then added HOBT (0.119 g, 1.1 eq.) followed by EDC HCl (0.150 g, 1.1 eq.) and oxazol-5-ylmethanamine HCl (0.143 g, 1.1 eq.). DIPEA (0.101 g, 1.1 eq) was added to this reaction mixture dropwise at the same temperature. The clear reaction mixture was stirred at 0° C. for 1.5 h. The progress of the reaction was followed by TLC analysis on silica gel with 5% methanol in dichloromethane as mobile phase and visualization with UV.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428490B2
Source datasetuspto-grants-2016_08
ORD IDord-f2c5e932c82a414c9ad86aef12395955
Source noteuspto-grants-2016_08