HCID 19027129, compound → HCID 19027149, compound
Reaction equation
[S:1]1[C:5]([C:6]2([OH:23])[C:15]3[C:10](=[CH:11][C:12]([O:16][CH3:17])=[CH:13][CH:14]=3)[CH2:9][CH:8]([C:18]([O:20][CH2:21][CH3:22])=[O:19])[CH2:7]2)=[CH:4][N:3]=[CH:2]1>C1C=CC2C(=CC=CC=2O)C=1>[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[C:6]1([OH:23])[C:15]2[C:10](=[CH:11][C:12]([O:16][CH3:17])=[CH:13][CH:14]=2)[CH2:9][CH:8]([C:18]([O:20][CH2:21][CH3:22])=[O:19])[CH2:7]1.[S:1]1[C:5]([C:6]2[C:15]3[C:10](=[CH:11][C:12]([OH:16])=[CH:13][CH:14]=3)[CH:9]=[C:8]([C:18]([O:20][CH3:21])=[O:19])[CH:7]=2)=[CH:4][N:3]=[CH:2]1Participants
4
Reactant 1
Product 2
Reagents, catalysts & solvents 1
Procedure
Following the procedure described in Naphthol 5, Steps 5-8, but substituting 1-(5-thiazolyl)-3-carbethoxy-6-methoxy-1,2,3,4-tetrahydro-1-naphthol from Step 1, for 1-(2-thiazolyl)-3-carbethoxy-6-methoxy-1,2,3,4-tetrahydro-1-naphthol, the title product was obtained as an orange solid.
Sources & evidence
- ORD record
- ord-4bb703b8db1544a48e7f64ed3b08e6ae
- Source dataset
- uspto-grants-1994_05
- Patent number
- US05308852
Reaction notes
Loading…