HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Fluorobenzo[c][1,2]oxaborole-1,5(3H)-diol → 5-Chloro-6-(6-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(2-isopropoxyethoxy)nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Fluorobenzo[c][1,2]oxaborole-1,5(3H)-diol | HCID 58079921 | — |
| Reactant | 5,6-Dichloro-2-(2-isopropoxyethoxy)nicotinonitrile | HCID 86661720 | — |
| Product | 5-Chloro-6-(6-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(2-isopropoxyethoxy)nicotinonitrile | HCID 66726550 | — |
Reaction Steps
This compound was prepared from 5,6-dichloro-2-(2-isopropoxyethoxy)nicotinonitrile and 6-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) 1.0 (d, J=4.5 Hz, 6H), 3.32-3.45 (m, 3H), 4.04-4.05 (m, 2H), 5.0 (s, 2H), 7.53 (d, J=4.8 Hz, 1H), 7.65 (d, J=7.2 Hz, 1H), 8.63 (s, 1H), 9.4 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145429B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-0f506e4c7c9d42f492712914e4cec801 |
| Source note | uspto-grants-2015_09 |