HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Thienylmethyl)amine → HCID 178518104, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Thienylmethyl)amine | HCID 34005 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 68819203 | HCID 68819203 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178518104 | HCID 178518104 | — |
Reaction Conditions
| Temperature | 145 °C |
|---|
Reaction Steps
The suspension of 2-methylsulfanyl-5-quinazolin-6-ylmethylene-thiazol-4-one (example 1c, 58 mg, 0.2 mmol), thiophene methyl amine (45.3 mg, 0.4 mmol) and diisopropylethylamine (DIEA) (70 uL, 0.4 mmol) in acetonitrile (1 mL) was heated to 145° C. by microwave for 20 min. After cooling to room temperature, the solid was collected by filtration, washed with a small amount of acetonitrile and dried. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 0%-5% methanol in methylene chloride in 30 min) afforded 5-[1-quinazolin-6-yl-meth-(Z)-ylidene]-2-[(thiophen-2-ylmethyl)-amino]-thiazol-4-one as a light yellow solid: LC-MS m/e 353 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501428B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-9e584cb90a00450092165bd64b716562 |
| Source note | uspto-grants-2009_03 |