Hydrazine hydrate (1:1) → cis-4-(3-Cyclopentyloxy-4-methoxyphenyl)-4a,5,8,8a-tetrahydro-2H-phthalazin-1-one
Reaction equation
O.NN.[CH3:4][O:5][C:6]1[CH:7]=[C:8]([C:14]2[C@H:23]3[C@H:18]([CH2:19][CH2:20][CH2:21][CH2:22]3)[C:17](=[O:24])[NH:16][N:15]=2)[CH:9]=[CH:10][C:11]=1[O:12][CH3:13]>>[CH:4]1([O:5][C:6]2[CH:7]=[C:8]([C:14]3[C@H:23]4[C@H:18]([CH2:19][CH:20]=[CH:21][CH2:22]4)[C:17](=[O:24])[NH:16][N:15]=3)[CH:9]=[CH:10][C:11]=2[O:12][CH3:13])[CH2:10][CH2:11][CH2:6][CH2:7]1Participants
3
Procedure
Prepared from compound E (see starting compounds) and hydrazine hydrate as described for compound 1. M.p. 166-168° C.
Sources & evidence
- ORD record
- ord-8ed947ff35c94c34a0f486c96d3103ed
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06103718
Reaction notes
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