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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486973Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 71493652, compound

https://huagongshe.com/reaction/1486973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-Ethyl-1-(pyridin-3-yl)ethan-1-amineHCID 14619192—
Reactant(Z)-3-(3-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,4-triazol-1-yl)acrylic acidHCID 86703006—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 71493652HCID 71493652145.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

In a 3-neck 50 mL round-bottomed flask, (Z)-3-(3-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,4-triazol-1-yl)acrylic acid (0.2 g, 1.0 eq.) was dissolved in dichloromethane (15 mL) at 0° C. under N2 atmosphere. To this reaction DIPEA (0.088 g, 1.2 eq.), EDC.HCl (0.131 g, 1.2 eq.) and N-ethyl-1-(pyridin-3-yl)ethanamine (0.102 g, 1.2 eq.) was added followed by HOBt (0.104 g, 1.2 eq.). Reaction mixture was stirred at 20° C. for 1 h. The progress of the reaction was followed by TLC analysis on silica gel with 10% methanol: dichloromethane as mobile phase and visualization with UV, SM Rf=0.15 and Product Rf=0.40. Reaction was stirred for 3-4 h and yellow reaction mixture was evaporated on rotary evaporator under reduced pressure to afford 0.4 g of crude compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428490B2
Source datasetuspto-grants-2016_08
ORD IDord-9e12b59c09544d24b6b597405b18b6cc
Source noteuspto-grants-2016_08