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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594922Generated: October 30, 2026

Dichloromethane → Acetamide, 2-(diethylamino)-N-(5-methyl-1,3,4-thiadiazol-2-yl)-

https://huagongshe.com/reaction/594922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantTrifluoroacetamideHCID 67717—
ReactantIodobenzene diacetateHCID 76724—
ReactantAcetamide, 2-(dimethylamino)-N-(5-propyl-1,3,4-thiadiazol-2-yl)-HCID 3076716—
ProductAcetamide, 2-(diethylamino)-N-(5-methyl-1,3,4-thiadiazol-2-yl)-HCID 3076717—

Reaction Steps

A mixture of AK-3 (1.0 g, 3.7 mmol), MgO (600 mg, 14.9 mmol), trifluoroacetamide (839 mg, 7.4 mmol), and Rh(II) acetate dimer (115 mg, 0.26 mmol) in DCM (10 mL) is added (diacetoxyiodo)benzene (1.79 g, 5.6 mmol). The mixture is stirred at rt for 18 h and then concentrated under reduced pressure. The resultant residue is dissolved in MeOH, filtered through a pad of diatomaceous earth and to it, K2CO3 (2.55 g, 18.6 mmol) is added. The mixture is stirred at rt for 18 h and is concentrated under reduced pressure. The resultant residue is purified by SiO2 flash chromatography to yield AK-4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242989B2
Source datasetuspto-grants-2016_01
ORD IDord-692e62c09d2e45bdaba1ddab76899a11
Source noteuspto-grants-2016_01