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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037006Generated: October 30, 2026

Hydrochloric Acid → N-((1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborol-5-yl)methyl)-2-methyl-4-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzamide

https://huagongshe.com/reaction/1037006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-Methyl-4-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzoic acidHCID 86685450—
ReactantHCID 86685451HCID 86685451—
SolventAcetonitrileHCID 6342—
ProductN-((1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborol-5-yl)methyl)-2-methyl-4-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzamideHCID 7157588025.2%

Reaction Steps

The solution of 2-methyl-4-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydro-isoxazol-3-yl)benzoic acid (300 mg, 0.665 mmol) and HATU (505.4 mg, 1.33 mmol) in CH3CN (15 mL) at rt was stirred for 5 min. The mixture was added to a solution of 5-(aminomethyl)-3,3-dimethylbenzo[c][1,2]oxaborol-1(3H)-ol hydrochloride (181.1 mg, 0.798 mmol) and TEA (268.7 mg, 2.66 mmol) in CH3CN (15 mL). Then the mixture was stirred at rt for 2 h. The solution was acidified with HCl (1 N) and extracted with EA. The combined organic layers were washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was purified by prep-TLC (PE:EA=2:1) to give the final title compound (105 mg, yield 25%): 1H NMR (300 MHz, DMSO-d6): δ 9.0 (s, 1H), 8.95 (t, 1H), 7.83 (s, 2H), 7.64-7.59 (m, 3 H), 7.47 (d, 1H), 7.34-7.29 (m, 2H), 4.52-4.50 (d, 2H), 4.37-4.34 (m, 2 H), 2.38 (s, 3H), 1.44 (s, 6 H); HPLC purity: 98.1% at 220 nm and 98.8% at 254 nm; MS: m/z=625 and 627 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546357B2
Source datasetuspto-grants-2013_10
ORD IDord-11bf6eb11b4e43bc82bb5411ced33a3d
Source noteuspto-grants-2013_10