HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575142Generated: October 29, 2026
Potassium Trifluoro(methyl)borate → 10-Bromo-9-fluoro-3-methyl-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide
https://huagongshe.com/reaction/575142
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Trifluoro(methyl)borate | HCID 23692566 | — |
| Reactant | 10-Bromo-9-fluoro-3-iodo-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide | HCID 86693052 | — |
| Product | 10-Bromo-9-fluoro-3-methyl-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide | HCID 89754685 | — |
Reaction Steps
10-Bromo-9-fluoro-3-iodo-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide (0.2 g) was reacted with potassium methyltrifluoroborate similar to as described in Example 5 to give 20 mg of 10-bromo-9-fluoro-3-methyl-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide after reverse phase hplc purification. This intermediate was reacted with 2-Methyl-3-butyne-ol similar to as described in Procedure E to afford 17.4 mg of 9-fluoro-3-[(2-fluorophenyl)methyl]-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide following reverse phase hplc purification. MS (Q1) 344 (M)+. 1H NMR (400 MHz, DMSO) δ 8.55 (dd, J=8.5, 3.5 Hz, 1H), 7.48 (s, 1H), 6.98 (d, J=10.5 Hz, 2H), 5.49 (s, 1H), 4.63-4.36 (m, 2H), 4.35-4.24 (m, 2H), 1.49 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034866B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-107a6b6e55694ed58ef0ea03dcdb92ba |
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| Source note | uspto-grants-2015_05 |
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