Benzyl Chloride → 1,2,3,3a-tetrahydro-5-(phenylmethyl)pyrrolo[1,2-a]quinoxalin-4(5H)-one
Reaction equation
[CH2:1]1[N:5]2[C:6]3[C:11]([NH:12][C:13](=[O:14])[CH:4]2[CH2:3][CH2:2]1)=[CH:10][CH:9]=[CH:8][CH:7]=3.[CH2:15](Cl)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[C:16]1([CH2:15][N:12]2[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[N:5]3[CH2:1][CH2:2][CH2:3][CH:4]3[C:13]2=[O:14])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1Participants
3
Procedure
Following the procedure of Example 2, 1,2,3,3a-tetrahydropyrrolo[1,2-a]quinoxalin-4(5H)-one is reacted with benzyl chloride to afford the title compound, m.p. 156°-157° C.
Sources & evidence
- ORD record
- ord-a1b68240ec6f493ab2ae659e573a3af1
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04446323
Reaction notes
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