HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12175809, compound → HCID 71008561, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12175809 | HCID 12175809 | — |
| Reactant | HCID 14762641 | HCID 14762641 | — |
| Product | HCID 71008561 | HCID 71008561 | 61% |
Reaction Steps
NMe2PY5Me2 was synthesized in a similar manner as that of CF3PY5Me2, using 1,1-bis(2-pyridyl)ethane and 4-dimethylamino-2,6-difluoropyridine as the precursors, and purified on a silica column eluted with CH2Cl2:MeOH:triethytamine (20:1:0.1). Yield: 61%. 1H NMR (CDCl3, 400 MHz): □ =8.44 (dd, J=4.81, 0.98 Hz, 4H), 7.28 (dt, J=7.86, 7.80, 1.89 Hz, 4H), 6.95 (ddd, J=7.41, 4.85, 0.98 Hz, 4H), 6.76 (d, J=8.05 Hz, 4H), 6.31 (s, 2H), 2.80 (s, 6H), 2.13 (s, 6H). Anal. Calcd. for C31H30N6: C, 76.52%; H, 6.21%; N, 17.27%. Found: C, 76.22%; H, 6.46%; N, 17.15%. LMS (M+) m/z calcd for [NMe2PY5Me2+H]+, 487.2610, found, 487.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575345B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-94b02b42b7ee496ab86f897ac7013afe |
| Source note | uspto-grants-2013_11 |