6639-66-3 → HCID 15227807, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[O:12][CH2:13][CH2:14][OH:15])[C:8](=O)[CH2:7][CH2:6]2.CC1C=CC(N=[CH:25][C:26]2[C:27]([NH2:35])=[CH:28][C:29]3[O:33][CH2:32][O:31][C:30]=3[CH:34]=2)=CC=1>>[OH:15][CH2:14][CH2:13][O:12][C:11]1[C:3]([O:2][CH3:1])=[CH:4][C:5]2[CH2:6][C:7]3[C:8]([C:9]=2[CH:10]=1)=[N:35][C:27]1[CH:28]=[C:29]2[O:33][CH2:32][O:31][C:30]2=[CH:34][C:26]=1[CH:25]=3Participants
3
Procedure
Using the procedure of Example 1, 5-methoxy-6-(2-hydroxyethoxy)indan-1-one (222 mg, 1 mmol) is reacted with 6[[(4-methylphenyl)imino]methyl]-1,3-benzodioxol-5-amine (255 mg, 1 mmol) to yields 7-(2-hydroxyethoxy)-8-methoxy-10H-1,3-dioxolo[4,5-g]indeno[1,2-b]quinoline (239 mg, 68% of theory).
Sources & evidence
- ORD record
- ord-d63df0e4cef940fa9b4ebccdcfcb209b
- Source dataset
- uspto-grants-1994_06
- Patent number
- US05318976
Reaction notes
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