Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | HCID 66710941 | HCID 66710941 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | HCID 66711042 | HCID 66711042 | 14% |
Reaction Steps
7-(5-Chloro-2-methoxy-phenyl)-2-methanesulfinyl-pyrrolo[2,1-f][1,2,4]triazine (75.0 mg, 0.000233 mol) and 4-Methoxybenzenamine (57.4 mg, 0.000466 mol) were dissolved in 2-Methoxyethanol (1.64 mL) and the reaction was heated at 180° C. until HPLC showed consumption of starting material. The reaction mixture was then reduced en vacuo and the product was isolated and purified by Gilson prep HPLC to afford 12.41 mg of [7-(5-Chloro-2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-(4-methoxy-phenyl)-amine as a lyophilized powder. (M+H)=381.11. 1H NMR (400 MHz, DMSO, d6) δ 9.29 (s, 1H), 8.95 (s, 1H), 8.05 (m, 1H), 7.63 (d, 2H, J=9.09 Hz), 7.46 (m, 1H), 7.23 (d, 1H, J=8.84 Hz), 7.03 (d, 1H, J=4.55 Hz), 6.90 (d, 1H, J=4.55 Hz), 6.85 (m, 2H), 3.82 (s, 3H), 3.70 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08471005B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-845f1672a19d4645bf50eb56a24b6b71 |
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| Source note | uspto-grants-2013_06 |
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