4-Hydroxy-3,5-bis(isopropyl)benzaldehyde → HCID 135406930, compound
Reaction equation
[CH:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([CH:13]([CH3:15])[CH3:14])[C:11]=1[OH:12])[CH:7]=O)([CH3:3])[CH3:2].[C:16]([CH2:18][C:19]([NH2:21])=[S:20])#[N:17]>>[NH2:21][C:19](/[C:18](=[CH:7]/[C:6]1[CH:5]=[C:4]([CH:1]([CH3:3])[CH3:2])[C:11]([OH:12])=[C:10]([CH:13]([CH3:15])[CH3:14])[CH:9]=1)/[C:16]#[N:17])=[S:20]Participants
3
Procedure
M25 was prepared using 3,5-diisopropyl-4-hydroxybenzaldehyde and cyanothioacetamide under similar conditions as described for M11.
Workup
- customwas prepared
Sources & evidence
- ORD record
- ord-7ffb4312dea741ab99a5641be70ca8eb
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06596878B2
Reaction notes
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