HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → HCID 58869947, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | HCID 16058694 | HCID 16058694 | — |
| Product | HCID 58869947 | HCID 58869947 | — |
Reaction Steps
The product from Example 1, Part C (350 mg, 1.1 mmol) and 2-aminothiazole (131 mg, 1.3 mmol) were converted to the title compound by the method described in Example 1, Part D (122 mg, 34%). 1H NMR (300 MHz, CDCl3) δ 7.37 (d, J=3.5 Hz, 1H); 7.22 (d, J=8.8 Hz, 2H); 7.02 (d, J=3.6 Hz, 1H); 7.22 (d, J=8.5 Hz, 2H); 5.11 (d, J=14.6 Hz, 1H); 4.61 (s, 1H); 4.17 (d, 14.6 Hz, 1H); 3.76 (s, 3H); 3.06 (s, 2H); 1.93 (s, 3H); 1.79 (s, 3H). MS: m/z (MH+) 404.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680122B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-12a121bcdd204cd0b2d04023dc13d4cf |
| Source note | uspto-grants-2014_03 |