Butanethiol → HCID 85326587, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:10][CH:9]2[NH:11][C:12]2[C:13]3[N:26]=[N:25][N:24]([CH:27]4[CH2:31][CH2:30][CH:29]([OH:32])[CH:28]4[OH:33])[C:14]=3[N:15]=[C:16]([S:18]([CH2:21][CH2:22][CH3:23])(=O)=O)[N:17]=2)=[CH:4][CH:3]=1.[CH2:34](S)CCC>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:10][CH:9]2[NH:11][C:12]2[C:13]3[N:26]=[N:25][N:24]([CH:27]4[CH2:31][CH2:30][CH:29]([OH:32])[CH:28]4[OH:33])[C:14]=3[N:15]=[C:16]([S:18][CH2:21][CH2:22][CH2:23][CH3:34])[N:17]=2)=[CH:4][CH:3]=1Participants
3
Procedure
The title compound was prepared as described in Example 8 using the product from step b) and butanethiol.
Sources & evidence
- ORD record
- ord-375cbccfadfa4276bad2d3611f6fc03b
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07034032B2
Reaction notes
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