HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Acetamide, 2-(diethylamino)-N-(5-methyl-1,3,4-thiadiazol-2-yl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trifluoroacetamide | HCID 67717 | — |
| Reactant | Iodobenzene diacetate | HCID 76724 | — |
| Reactant | Acetamide, 2-(dimethylamino)-N-(5-propyl-1,3,4-thiadiazol-2-yl)- | HCID 3076716 | — |
| Product | Acetamide, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242989B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-692e62c09d2e45bdaba1ddab76899a11 |
| Source note | uspto-grants-2016_01 |