HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Pyridin-2-ylphenyl)methanamine → HCID 70222420, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Pyridin-2-ylphenyl)methanamine | HCID 22337704 | — |
| Reactant | HCID 25210248 | HCID 25210248 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70222420 | HCID 70222420 | 60% |
Reaction Steps
According to the same conditions resulting in the preparation of the compound IIa.1, the compound IIa.2 is prepared from 8-isopropyl-4-(N-methyl-N-phenylamino)-2-(methylsulfanyl)pyrazolo[1,5-a]-1,3,5-triazine and from 4-(pyridin-2-yl)benzylamine. Yield=60%. Mp=136-138° C. (EtOH). 1H NMR (300 MHz, CDCl3): δ 8.71 (d, 1H, J=4.7 Hz, Harom), 8.00 (d, 2H, J=8.1 Hz, Harom), 7.82-7.72 (m, 3H, Harom), 7.49 (d, 2H, J=8.1 Hz, Harom), 7.26 (dd, 1H, J=4.7 Hz, 7.2 Hz, Harom), 6.76 (bs, 1H, NH), 4.86 (d 2H, J=6.0 Hz, CH2), 3.16 (hept, 1H, J=7.0 Hz, CH), 2.57 (s, 3H, CH3), 1.33 (d, 6H, J=7.0 Hz, 2 CH3). MS (ESI): m/z 391 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691982B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-8d90a5c3b88e42588babad611727cfa6 |
| Source note | uspto-grants-2014_04 |