tert-Butyl carbazate → HCID 68934180, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4](/[CH:8]=[CH:9]/[C:10]2[C:18]3[C:13](=[CH:14][CH:15]=[C:16]([C:21](O)=[O:22])[C:17]=3[O:19][CH3:20])[N:12]([C:24]([C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=3)([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=3)[C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[N:11]=2)[CH:5]=[CH:6][CH:7]=1.[C:43]([O:47][C:48]([NH:50][NH2:51])=[O:49])([CH3:46])([CH3:45])[CH3:44]>>[C:43]([O:47][C:48]([NH:50][NH:51][C:21]([C:16]1[C:17]([O:19][CH3:20])=[C:18]2[C:13](=[CH:14][CH:15]=1)[N:12]([C:24]([C:37]1[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=1)([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1)[N:11]=[C:10]2/[CH:9]=[CH:8]/[C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([F:1])[CH:3]=1)=[O:22])=[O:49])([CH3:46])([CH3:45])[CH3:44]Participants
3
Procedure
94 mg of 3-[(E)-2-(3-fluorophenyl)-vinyl]-4-methoxy-1-trityl-1H-indazole-5-carboxylic acid and 34.4 mg of hydrazine carboxylic acid tert-butyl ester were condensed in the manner as described in Example 127, to afford 126.9 mg of the title compound as pale yellow crude crystals.
Workup
- customcondensed in the manner
Sources & evidence
- ORD record
- ord-5bf5f345cacb46b0977ef51861d239d9
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07429609B2
Reaction notes
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