HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-chloro-N-(fluoren-9-yl)-5-fluoro-4-pyrimidineamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4-Dichloro-5-fluoropyrimidine | HCID 250705 | — |
| Reactant | 9H-fluoren-9-amine hydrochloride | HCID 2724685 | — |
| Product | 2-chloro-N-(fluoren-9-yl)-5-fluoro-4-pyrimidineamine | HCID 22060636 | — |
Reaction Steps
In like manner to the preparation of 2-chloro-N4-(3,4-ethylenedioxyphenyl)-5-fluoro 4-pyrimidineamine, 9-aminofluorene hydrochloride and 2,4-dichloro-5-fluoropyrimidine with added diisopropylethylamine were reacted to produce 2-chloro-N-(fluoren-9-yl)-5-fluoro-4-pyrimidineamine. 1H NMR (CDCl3): δ 7.97 (d, 1H, J=2.3 Hz), 7.73 (d, 2H, J=7.6 Hz), 7.59 (d, 2H, J=7.6 Hz), 7.44 (t, 2H, J=7.6 Hz), 7.32 (app t, 2H, J=7.6 Hz), 6.50 (d, 1H, J=8.8 Hz), 5.45 (d, 1H, J=8.4 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08334296B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-083063559e0c4dff807a9628422e2c6e |
| Source note | uspto-grants-2012_12 |