HCID 13151869, compound → HCID 15661031, compound
Reaction equation
[C:1]([C:4]1[CH:23]=[CH:22][C:7]2[S:8](=[O:21])(=[O:20])[C:9]3[CH:16]=[C:15]([C:17]([OH:19])=[O:18])[CH:14]=[CH:13][C:10]=3[CH2:11][CH2:12][C:6]=2[CH:5]=1)(=[O:3])[CH3:2].[C:24](C1C=CC2SC3C=C(C(O)=O)C=CC=3CCC=2C=1)(=O)C>>[C:1]([C:4]1[CH:23]=[CH:22][C:7]2[S:8](=[O:21])(=[O:20])[C:9]3[CH:16]=[C:15]([C:17]([O:19][CH3:24])=[O:18])[CH:14]=[CH:13][C:10]=3[CH2:11][CH2:12][C:6]=2[CH:5]=1)(=[O:3])[CH3:2]Participants
3
Procedure
Following the procedure described in Example 10, Step 1, but substituting 2-acetyl-5,5-dioxo-10,11-dihydrodibenzo[b,f]thiepin-7-carboxylic acid (U.S. Pat. No. 4,536,507 (1985)) for 2-acetyl-10,11-dihydrodibenzo[b,f]thiepin-7-carboxylic acid as starting material, the title product was obtained as a solid.
Sources & evidence
- ORD record
- ord-9cd43175124a427090a7cc7b5fa2a728
- Source dataset
- uspto-grants-1991_07
- Patent number
- US05036067
Reaction notes
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