HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-bromo-N-cyclopropyl-4-Thiazolecarboxamide → HCID 136348497, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-bromo-N-cyclopropyl-4-Thiazolecarboxamide | HCID 15009547 | — |
| Reactant | HCID 68328163 | HCID 68328163 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 136348497 | HCID 136348497 | 30% |
Reaction Steps
The title compound (34 mg, 30% yield) as a yellow crystalline solid was prepared according to Example 275, using N-isopropyl-5-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-indol-5-yl)-1,3,4-oxadiazol-2-amine (145 mg, 0.278 mmol), 2-bromo-N-cyclopropylthiazole-4-carboxamide (75 mg, 0.305 mmol), and Pd(PPh3)4 (Strem Chemicals, 16 mg) as the starting materials and reagent. 1H NMR (400 MHz, DMSO-d6) δ ppm 12.15 (1H, br.), 8.57 (1H, s), 8.29 (2H, m), 8.15 (1H, s), 7.74 (1H, d, J=7.4 Hz), 7.65 (2H, d, J=8.6 Hz), 3.77 (1H, m), 2.90 (1H, m), 1.25 (6H, d, J=6.1 Hz), 0.75 (2H, m.), 0.69 (2H, m). MS (ESI, pos. ion) m/z 409.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321756B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-9ad8758fd6b34d47a12945766dbc76d9 |
| Source note | uspto-grants-2016_04 |