HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-fluorobenzo[c][1,2]oxaborole-1,5(3H)-diol → 6-(7-Fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(2-isopropoxyethoxy)-4-(trifluoromethyl)nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-fluorobenzo[c][1,2]oxaborole-1,5(3H)-diol | HCID 58079919 | — |
| Reactant | 6-Chloro-2-(2-isopropoxyethoxy)-4-(trifluoromethyl)nicotinonitrile | HCID 86661735 | — |
| Product | 6-(7-Fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(2-isopropoxyethoxy)-4-(trifluoromethyl)nicotinonitrile | HCID 66726475 | — |
Reaction Steps
This compound was prepared from 6-chloro-2-(2-isopropoxyethoxy)-4-(trifluoromethyl)nicotinonitrile and 7-fluorobenzo[c][1,2]oxaborole-1,5(3H)-diol in a similar manner to that of D230. 1H-NMR (400 MHz, DMSO-d6) δ (ppm) 1.06 (d, J=6 Hz, 6H), 3.52-3.55 (m, 1H), 3.59-3.61 (t, J=4.8 Hz, 2H), 4.26-4.28 (t, J=4.8 Hz, 2H), 5.07 (s, 2H), 7.18 (d, J=8.0 Hz, 1H), 7.27 (s, 1H), 7.38 (s, 1H), 9.39 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145429B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-ab61e2c43ade4d76812ba9f8b96755d0 |
| Source note | uspto-grants-2015_09 |