HCID 21828801, compound → HCID 22449474, compound
Reaction equation
[C:1]([NH:4][C:5]1[CH:14]=[CH:13][C:12]([Cl:15])=[C:11]2[C:6]=1[C:7](=[O:16])[CH2:8][CH2:9][S:10]2)(=[O:3])[CH3:2].[C:17]([NH:20]C1C=CC(C)=C2C=1C(=O)CCS2)(=[O:19])[CH3:18]>>[C:17]([NH:20][CH:8]1[C:7](=[O:16])[C:6]2[C:11](=[C:12]([Cl:15])[CH:13]=[CH:14][C:5]=2[NH:4][C:1](=[O:3])[CH3:2])[S:10][CH2:9]1)(=[O:19])[CH3:18]Participants
3
Procedure
The reaction was carried out in the same manner as in Example 12-(1), except that 477 mg of the compound prepared in (1) above was used instead of 5-acetylamino-8-methyl-4-thiochromanone of Example 12-(1). The reaction product was post-treated to produce 171 mg of the title compound.
Workup
- additionThe reaction product was post-treated
Sources & evidence
- ORD record
- ord-0fc83c9efec64d57816ba07544250764
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05770605
Reaction notes
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