Acetic Acid → HCID 178481357, compound
Reaction equation
Br[CH2:2][C:3]([C:5]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:6]=1[C:7]1([C:27]3[C:18](=[CH:19][C:20]4[O:25][CH2:24][CH2:23][O:22][C:21]=4[CH:26]=3)[O:17][CH2:16]1)[C:8](=[O:15])[N:9]2[CH3:14])=O.[OH2:28].[NH2:29][NH2:30].[C:31](O)(=O)C>>[OH:28][C:31]1[NH:30][N:29]=[C:3]([C:5]2[CH:13]=[CH:12][CH:11]=[C:10]3[C:6]=2[C:7]2([C:27]4[C:18](=[CH:19][C:20]5[O:25][CH2:24][CH2:23][O:22][C:21]=5[CH:26]=4)[O:17][CH2:16]2)[C:8](=[O:15])[N:9]3[CH3:14])[CH:2]=1Participants
Procedure
To a suspension of 4′-(bromoacetyl)-1′-methyl-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-2′(1′H)-one (0.23 g, 0.53 mmol) in glacial acetic acid (5 mL) was added dropwise hydrazine hydrate (0.03 mL, 0.59 mmol) and the reaction mixture was heated at reflux for 16 h, allowed to cool to ambient temperature and was concentrated in vacuo. The crude product was triturated in dichloromethane (10 mL) and the resultant solid was recrystallized from dichloromethane/diethyl ether. Following a second recrystallization from methanol, 4′-(5-hydroxy-1H-pyrazol-3-yl)-1′-methyl-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-2′(1′H)-one (0.029 g, 14%) was obtained as a colorless solid: mp>250° C. (methanol); 1H NMR (300 MHz, DMSO-d6) δ 11.77 (br s, 1H), 9.51 (br s, 1H), 7.49-7.39 (m, 1H), 7.22-7.09 (m, 2H), 6.41 (s, 1H), 6.15 (s, 1H), 4.76-4.42 (m, 3H), 4.25-4.02 (m, 4H), 3.19 (s, 3H); 13C NMR (75 MHz, DMSO-d6) δ 177.1, 155.0, 144.7, 144.0, 137.2, 129.1, 126.5, 123.1, 121.8, 110.6, 108.8, 98.7, 90.6, 76.2, 64.2, 63.6, 57.7, 26.5; MS (ES+) m/z 391.8 (M+1).
Workup
- temperaturethe reaction mixture was heated
- temperatureat reflux for 16 h
- concentrationwas concentrated in vacuo
- customThe crude product was triturated in dichloromethane (10 mL)
- customthe resultant solid was recrystallized from dichloromethane/diethyl ether
- customa second recrystallization from methanol
Sources & evidence
- ORD record
- ord-119c3bf32d3a452c878fa8db185295c0
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263606B2
Reaction notes
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