HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-morpholino-6,7,8,9-tetrahydro-5H-benzo[7]annulen-3-amine → HCID 66829766, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-morpholino-6,7,8,9-tetrahydro-5H-benzo[7]annulen-3-amine | HCID 57416136 | — |
| Reactant | 2-((2-Chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)-N-methylbenzamide | HCID 86633861 | — |
| Product | HCID 66829766 | HCID 66829766 | — |
Reaction Steps
The title compound was prepared from 2-(2-chloro-5-trifluoromethyl-pyrimidin-4-ylamino)-N-methyl-benzamide and 7-morpholin-4-yl-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-ylamine in an analogous manner to Example 195 (microwave: 120° C., 60 minutes) to afford an off-white solid (35 mg, 86%). Mp: 158-62° C. LCMS (m/e) 541 (M+1); 1H-NMR (CDCl3, 400 MHz) δ 10.85 (s, 1H), 8.45 (d, J=9 Hz, 1H), 8.36 (s, 1H), 7.50 (d, J=7 Hz, 1H), 7.47-7.37 (m, 2H), 7.30 (m, 1H), 7.25 (m, 2H), 7.10 (m, 1H), 6.27 (br s, 1H), 3.90-3.70 (m, 4H), 3.04 (s, 3H), 2.90-2.50 (m, 7H), 2.17 (m, 2H), 1.80-1.35 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552186B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-ec103adeb79847038efaa9c43900d535 |
| Source note | uspto-grants-2013_10 |