HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azetidine → HCID 72547727, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | HCID 72547722 | HCID 72547722 | — |
| Product | HCID 72547727 | HCID 72547727 | 47% |
Reaction Steps
Reaction of azetidine with 2-((6-chloro-4-(1-(oxetan-3-yl)piperidin-4-yl)pyridin-2-yl)amino)isonicotinonitrile (40 mg, 0.11 mmol) following general Buchwald-Hartwig procedure described above afforded the target compound as a colorless solid (19.8 mg, 47%); 1H NMR (400 MHz, DMSO) δ 9.76 (br s, 1H), 8.51 (s, 1H), 8.40 (d, J=5.1 Hz, 1H), 7.18 (d, J=5.1 Hz, 1H), 6.59 (s, 1H), 5.80 (s, 1H), 4.57-4.49 (m, 2H), 4.49-4.40 (m, 2H), 4.00-3.92 (m, 4H), 3.43-3.35 (m, 1H), 2.82-2.73 (m, 2H), 2.40-2.27 (m, 3H), 1.88-1.78 (m, 2H), 1.77-1.68 (m, 2H), 1.68-1.51 (m, 2H); ESI-LRMS m/z [M+1]+=391.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09399636B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-21ce8af432bd4530b8e717a1f2b1585c |
| Source note | uspto-grants-2016_07 |