HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → 7-Methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 7-Methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-one | HCID 597065 | 48.2% |
Reaction Steps
A solution of 2-aminothiazole (50 g, 499.301 mmol), ethyl acetoacetate (96 ml, 748.885 mmol) and acetic acid (400 ml) was reacted together according to the procedure described in Intermediate 3, Step 1 to afford a crude product which was purified by silica gel column chromatography using 1% methanol in chloroform to give 40 g of the product as a white solid; 1H NMR (300 MHz, CDCl3) δ 2.38 (s, 3H), 6.15 (s, 1H), 6.95 (d, J=4.8 Hz, 1H), 7.94 (d, J=4.8 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518955B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-afabc9c2256945ddbad32f6c5b02c61f |
| Source note | uspto-grants-2013_08 |