HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-benzyl-2-(4-bromobutanamido)-4-methylthiazole-5-carboxamide → HCID 16954475, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-benzyl-2-(4-bromobutanamido)-4-methylthiazole-5-carboxamide | HCID 86638730 | — |
| Reactant | 2-(4-bromobutanamido)-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide | HCID 86638731 | — |
| Product | HCID 16954475 | HCID 16954475 | 85% |
Reaction Steps
Following the procedure as described in Example 1, making variations as required to use 2-(4-bromobutanamido)-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide in replace of N-benzyl-2-(4-bromobutanamido)-4-methylthiazole-5-carboxamide, the title compound was obtained as a white solid in 85% yield: 1H NMR (300 MHz, CD3OD) δ 7.39-7.33 (m, 2H), 7.09-7.02 (m, 2H), 4.48 (s, 2H), 4.15-4.09 (m, 2H), 2.68 (t, J=8.1 Hz, 2H), 2.55 (s, 3H), 2.25 (m, 2H); MS (ES+) m/z 334.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08236835B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-2d4fb5d33101441fb45e966a89e18f3a |
| Source note | uspto-grants-2012_08 |