Sodium Hydroxide → HCID 21920742, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([O:11]C)=[O:10])=[CH:4][C:3]=1[NH:13][C:14]([NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=1)=[O:15].[OH-].[Na+]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=[O:10])=[CH:4][C:3]=1[NH:13][C:14]([NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=1)=[O:15]Participants
3
Procedure
For ester cleavage, 2.47 mmol (790 mg) of methyl 4-chloro-3-[[(2-pyridinylamino)carbonyl]amino]benzeneacetate is saponified with 1N NaOH analogously to the instructions above. Product 7 is obtained without recrystallization. Yield: 693 mg of yellowish solid.
Sources & evidence
- ORD record
- ord-f894ba81bb254d0382d0d50f4fe9c6fe
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07122570B2
Reaction notes
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