Hydrochloric Acid → HCID 18663206, compound
Reaction equation
[F:1][C:2]1[CH:30]=[CH:29][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][N:17]4[CH2:21][CH2:20][N:19]([C:22]5[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=5)[C:18]4=[O:28])[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1.[CH2:31]([O:33]C1C=CC=CC=1N=C=O)[CH3:32].Cl>>[F:1][C:2]1[CH:30]=[CH:29][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][N:17]4[CH2:21][CH2:20][N:19]([C:22]5[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=5[O:33][CH2:31][CH3:32])[C:18]4=[O:28])[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1Participants
4
Procedure
This product is obtained in the same manner as the compound of Example 5, but with replacement of the phenyl isocyanate by 2-ethoxyphenyl isocyanate in Step 1 of the synthesis. The hydrochloride of the title compound melts at 214°-218° C.
Sources & evidence
- ORD record
- ord-8ca663c865014ce08e4330761917f573
- Source dataset
- uspto-grants-1998_07
- Patent number
- US05780474
Reaction notes
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