HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037019Generated: October 30, 2026
Diisopropylethylamine → HCID 71575945, compound
https://huagongshe.com/reaction/1037019
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 4-(5-(3,5-Dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-2-methylbenzoic acid | HCID 86685453 | — |
| Reactant | HCID 86685457 | HCID 86685457 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 71575945 | HCID 71575945 | 61.3% |
Reaction Steps
To a solution of 4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-2-methylbenzoic acid (3.6 g, 8.3 mmol) and HATU (5.24 g, 13.8 mmol) in DMF (25 mL) was added DIPEA (3.3 mL, 18.4 mmol). The reaction mixture was stirred at rt for 10 min and 6-(aminomethyl)-3,3-dimethylbenzo[c][1,2]oxaborol-1(3H)-ol hydrochloride (2.1 g, 9.2 mmol) was added. The reaction mixture was stirred overnight. Water was added and the mixture was extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography over silica gel eluted with PE:EA (3:1 to 1:1) to give the final title compound 4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N-((1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)methyl)-2-methylbenzamide (3.1 g; yield 61%) as a white solid. 1H NMR (500 MHz, DMSO-d6) δ 9.08 (s, 1H), 8.94 (t, J=6.0 Hz, 1H), 7.84 (d, J=6.5 Hz, 2H), 7.66-7.62 (m, 3H), 7.53-7.43 (m, 3H), 4.49 (d, J=6.0 Hz, 2H), 4.39 (d, J=18.5 Hz, 1H), 4.36 (d, J=18.5 Hz, 1 H), 2.42 (s, 3 H), 1.47 (s, 6H) ppm; HPLC purity: 100% at 220 nm and 99.75% at 254 nm; MS: m/z=608.8 (M+1, ESI+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546357B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-d6aa66c3e5424fe28ba74efab9512f3d |
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| Source note | uspto-grants-2013_10 |
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