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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894905Generated: November 1, 2026

Triethylamine → N-(5-iodo-6-methylpyridin-3-yl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1894905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
Reactant5-Iodo-6-methylpyridin-3-amineHCID 59198291—
SolventDichloromethaneHCID 6344—
ProductN-(5-iodo-6-methylpyridin-3-yl)-3-(trifluoromethyl)benzamideHCID 69042846—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-iodo-6-methylpyridin-3-amine (125 mg, 0.534 mmol) in methylene chloride (1 mL) was added triethylamine (0.087 mL, 0.627 mmol) and cooled at 0° C. Into the reaction was added 3-(trifluoromethyl)benzoyl chloride (0.0812 mL, 0.538 mmol) dropwise and stirred at 0° C. for 45 minutes and at 25° C. for 16 hours. The reaction was extracted with EtOAc and the organic extracts were washed with water saturated Na2CO3, saturated NaCl, dried (MgSO4) and stripped in vacuo. The product was used in the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513270B2
Source datasetuspto-grants-2013_08
ORD IDord-fdd556997cbd490fa4e181c61ae4a092
Source noteuspto-grants-2013_08