[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[C:11]([NH2:13])[CH:12]=1)[NH:9][CH2:8][CH:7]([N:14]([CH3:16])[CH3:15])[CH2:6]2.NC1C=CC=C2C=1NCC(N[C:29](=O)[O:30]C(C)(C)C)C2>>[CH3:16][N:14]([CH3:15])[CH:7]1[CH2:6][C:5]2[C:10]3=[C:11]([NH:13][C:29](=[O:30])[N:9]3[CH2:8]1)[CH:12]=[C:3]([O:2][CH3:1])[CH:4]=2This compound was prepared by following the procedure of Example 44 part B, but substituting, 1,2,3,4-tetrahydro-6methoxy-N3,N3 -dimethyl- 3,8-quinolinediamine for t-butyl (8-amino-1,2,3,4-tetrahydro-3-quinolyl)carbamate.
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