Acetic Acid → HCID 178433372, compound
Reaction equation
[C:1]([CH2:3][C:4]1[CH:18]=[CH:17][C:7]([CH2:8][CH:9]([C:14](=O)[CH3:15])[C:10](OC)=[O:11])=[CH:6][CH:5]=1)#[N:2].[NH2:19][C:20]([NH2:22])=[NH:21].C(O)(=O)C>CCO>[NH2:22][C:20]1[N:21]=[C:10]([OH:11])[C:9]([CH2:8][C:7]2[CH:17]=[CH:18][C:4]([CH2:3][C:1]#[N:2])=[CH:5][CH:6]=2)=[C:14]([CH3:15])[N:19]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of the crude product from step (i) and guanidine (16 g) in EtOH (350 ml) was heated under reflux for 5 h. The mixture was cooled, neutralised with acetic acid, and the solid filtered and dried, 22.1 g.
Workup
- temperaturewas heated
- temperatureunder reflux for 5 h
- temperatureThe mixture was cooled
- filtrationthe solid filtered
- customdried
Sources & evidence
- ORD record
- ord-5b16fe2b445c4de69d59080041956064
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08268990B2
Reaction notes
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