HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[4-(Thiophen-3-yl)phenyl]methanamine → HCID 68109328, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[4-(Thiophen-3-yl)phenyl]methanamine | HCID 18525830 | — |
| Reactant | HCID 25210248 | HCID 25210248 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68109328 | HCID 68109328 | 74% |
Reaction Steps
According to the same conditions resulting in the preparation of the compound IIa.1, the compound IIa.3 is prepared from 8-isopropyl-4-(N-methyl-N-phenylamino)-2-(methylsulfanyl)pyrazolo[1,5-a]-1,3,5-triazine and from 4-(thiophen-3-yl)benzylamine. Yield=74%. Mp=141-143° C. (EtOH). 1H NMR (300 MHz, CDCl3): δ 7.73 (s, 1H, Harom), 7.57 (d, 2H, J=8.3 Hz, Harom), 7.45-7.36 (m, 5H, Harom), 6.78 (bs, 1H, NH), 4.81 (d, 2H, J=6.0 Hz, CH2), 3.16 (hept, 1H, J=7.0 Hz, CH), 2.58 (s, 3H, CH3), 1.33 (d, 6H, J=7.0 Hz, 2 CH3). MS (ESI): m/z 396 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691982B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-750637fba71b4652a01be49e53d05669 |
| Source note | uspto-grants-2014_04 |