HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminopyrazine → HCID 57470995, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminopyrazine | HCID 78747 | — |
| Reactant | 3,5-Dibromobenzamide | HCID 2735937 | — |
| Product | HCID 57470995 | HCID 57470995 | — |
Reaction Steps
3,5-Dibromo-benzamide and pyrazin-2-ylamine were coupled to give 3-bromo-5-(pyrazin-2-ylamino)-benzamide as described for Example 44. 3-Bromo-5-(pyrazin-2-ylamino)-benzamide was converted to 3-(1H-indol-4-yl)-5-(pyrazin-2-ylamino)-benzamide as described in Example 75. 1H NMR (400 MHz, CDCl3): δ 10.61 (s, 1H), 8.24 (t, J=1.8 Hz, 1H), 8.17-8.12 (m, 3H), 8.06 (s, 1H), 7.88 (s, 1H), 7.78 (t, J=1.5 Hz, 1H), 7.40 (dd, J=6.6, 2.1 Hz, 1H), 7.30 (d, J=3.1 Hz, 1H), 7.21-7.16 (m, 2H), 6.74 (d, J=2.7 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504401B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-029a39d51ba24a0fbc2a74494c6e0b6d |
| Source note | uspto-grants-2009_03 |