Isaglidole → HCID 70407469, compound
Reaction equation
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH2:4][N:5]([NH:11][C:12]1[NH:13][CH2:14][CH2:15][N:16]=1)[CH2:6]2.[C:17]([OH:24])(=[O:23])/[CH:18]=[CH:19]\[C:20]([OH:22])=[O:21]>C(OCC)(=O)C>[C:17]([OH:24])(=[O:23])/[CH:18]=[CH:19]\[C:20]([OH:22])=[O:21].[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH2:4][N:5]([NH:11][C:12]1[NH:13][CH2:14][CH2:15][N:16]=1)[CH2:6]2Participants
4
Reagents, catalysts & solvents 1
Procedure
2.0 g of the base (Example 1) are dissolved in 100 ml of hot ethyl acetate and a hot solution of 1 g of maleic acid in ethyl acetate is added.
Sources & evidence
- ORD record
- ord-15cfdb73000b452c9a5f0276fdb5ba78
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04777181
Reaction notes
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