HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-methoxyphenyl)-N-methylmethanamine → HCID 24954701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-methoxyphenyl)-N-methylmethanamine | HCID 485407 | — |
| Reactant | 1-(4-fluorophenyl)-N-methylmethanamine | HCID 736860 | — |
| Reactant | 2-(6-Iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid 4-fluoro benzylamide | HCID 86645558 | — |
| Product | HCID 24954701 | HCID 24954701 | 72% |
Reaction Steps
Following the procedure described in Example 14, making variations as required to replace 4-fluoro-N-methyl-benzylamine with (4-methoxy-benzyl)-methyl-amine to react with 2-(6-iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid 4-fluoro benzylamide, the title compound was obtained in 72% yield. 1H NMR (400 MHz, CD2Cl2) δ 8.55 (s, 1H), 8.06 (s, 1H), 7.29-7.37 (m, 2H), 7.17-7.24 (m, 2H), 6.99-7.07 (m, 2H), 6.80-6.87 (m, 2H), 6.20 (bs, 1H), 4.75 (s, 2H), 4.53 (d, J=4.0 Hz, 2H), 3.74 (s, 3H), 3.11 (s, 3H), 2.70 (s, 3H); MS (ES+) m/z 478.2 (M+1), Rt=1.58 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314138B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-8eeccc1e67434b1ca30fa164a8c09d30 |
| Source note | uspto-grants-2012_11 |