Sodium Hydroxide → HCID 21920861, 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][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=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][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:15]Participants
3
Procedure
For ester cleavage, analogously to the above instructions, 2.47 mmol (790 mg) of methyl 4-chloro-3-[[[(phenylmethyl)amino]carbonyl]amino]benzeneacetate is saponified with 1N-NaOH. Product 5 is obtained without recrystallization. Yield: 693 mg of yellowish solid.
Sources & evidence
- ORD record
- ord-099b41f3251a4819a92eddcc8dfbd7a3
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07122570B2
Reaction notes
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