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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284523Generated: October 29, 2026

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

https://huagongshe.com/reaction/2284523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-fluorobenzo[c][1,2]oxaborole-1,5(3H)-diolHCID 58079919—
Reactant6-Chloro-2-(2-isopropoxyethoxy)-4-(trifluoromethyl)nicotinonitrileHCID 86661735—
Product6-(7-Fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(2-isopropoxyethoxy)-4-(trifluoromethyl)nicotinonitrileHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145429B2
Source datasetuspto-grants-2015_09
ORD IDord-ab61e2c43ade4d76812ba9f8b96755d0
Source noteuspto-grants-2015_09