Hydrochloric Acid → HCID 54423886, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:33])[C:4]([N:19]=C(C1C=CC=CC=1)C1C=CC=CC=1)([CH2:12][C:13]1[N:14]([CH3:18])[CH:15]=[N:16][CH:17]=1)[CH2:5][C:6]1[N:7]([CH3:11])[CH:8]=[N:9][CH:10]=1.Cl>C1COCC1>[CH3:1][O:2][C:3](=[O:33])[C:4]([NH2:19])([CH2:12][C:13]1[N:14]([CH3:18])[CH:15]=[N:16][CH:17]=1)[CH2:5][C:6]1[N:7]([CH3:11])[CH:8]=[N:9][CH:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Using the same procedure as described in Example 53B, the title compound of 56A (960 mg, 2.17 mmol) was treated with HCl in THF to afford the title compound of 56B, 652 mg (77% yield).
Sources & evidence
- ORD record
- ord-77422b20e139401ea10f86ba5251efc9
- Source dataset
- uspto-grants-2001_02
- Patent number
- US06194438B1
Reaction notes
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