HCID 19086216, compound → HCID 19027165, compound
Reaction equation
[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[C:6]1[C:15]2[C:10](=[CH:11][C:12]([O:16][CH3:17])=[CH:13][CH:14]=2)[CH:9]=[C:8]([C:18]([O:20]CC)=[O:19])[CH:7]=1>C1C=C2C=CC=C(O)C2=CC=1>[C:2]1([C:6]2[C:15]3[C:10](=[CH:11][C:12]([O:16][CH3:17])=[CH:13][CH:14]=3)[CH:9]=[C:8]([C:18]([OH:20])=[O:19])[CH:7]=2)[CH:14]=[CH:15][CH:6]=[CH:7][CH:8]=1.[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[C:6]1[C:15]2[C:10](=[CH:11][C:12]([OH:16])=[CH:13][CH:14]=2)[CH:9]=[C:8]([C:18]([OH:20])=[O:19])[CH:7]=1Participants
4
Reactant 1
Product 2
Reagents, catalysts & solvents 1
Procedure
Following the procedure described in Naphthol 1, Step 3, but substituting 1-(2-thiazolyl)-3-carbethoxy-6-methoxynaphthalene from Step 6, for 1-phenyl-3-carboxy-6-methoxynaphthalene, the title product was obtained and used as such for the next step.
Sources & evidence
- ORD record
- ord-99b3eb35e5d64ef6ab163f0ce82d948c
- Source dataset
- uspto-grants-1994_05
- Patent number
- US05308852
Reaction notes
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