HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-bromo-N-(4-methylpent-2-yn-4-yl)butyramide → 2-(3-cyano-6-quinolinyloxy)-N-(4-methylpent-2-yn-4-yl) butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-bromo-N-(4-methylpent-2-yn-4-yl)butyramide | HCID 21078406 | — |
| Reactant | 6-Hydroxy-3-quinolinecarbonitrile | HCID 21923141 | — |
| Product | 2-(3-cyano-6-quinolinyloxy)-N-(4-methylpent-2-yn-4-yl) butyramide | HCID 69254688 | — |
Reaction Steps
In a similar procedure to Example 6 Stage 2, 3-cyano-6-hydroxyquinoline was reacted with 2-bromo-N-(4-methylpent-2-yn-4-yl) butyramide to give 2-(3-cyano-6-quinolinyloxy)-N-(4-methylpent-2-yn-4-yl) butyramide as a pale yellow solid, m.p. 116-118° C., 1H NMR (CDCl3) δ: 1.08(3H, t); 1.61(3H, s); 1.63(3H, s); 1.80(3H, s); 2.07-2.13(2H, m); 4.72(1H, t); 6.46(1H, s); 7.50 (1H, m); 7.57(1H, dd); 7.71(1H, d); 8.17(1H,d); 8.92(1H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07371764B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-2dcc38aa240a4b02a4c3af4605544243 |
| Source note | uspto-grants-2008_05 |