Acetic Acid → HCID 20086526, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]([NH:9][C:10]([C:12]2([CH3:32])[CH2:17][CH2:16][C:15]3[C:18]([CH3:31])=[C:19]([O:24][CH2:25][C:26]([O:28]CC)=[O:27])[C:20]([CH3:23])=[C:21]([CH3:22])[C:14]=3[O:13]2)=[S:11])[CH:3]=1.[OH-].[Na+].C(O)(=O)C>C(O)C.O>[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]([NH:9][C:10]([C:12]2([CH3:32])[CH2:17][CH2:16][C:15]3[C:18]([CH3:31])=[C:19]([O:24][CH2:25][C:26]([OH:28])=[O:27])[C:20]([CH3:23])=[C:21]([CH3:22])[C:14]=3[O:13]2)=[S:11])[CH:3]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
1.77 grams (4 mmol) of the compound of Example 67 are dissolved in 40 cm3 of ethanol. 4 cm3 of 2N sodium hydroxide are added dropwise. The mixture is stirred for 2 hours, then the reaction mixture is diluted with 60 cm3 of water and acidified with acetic acid. The mixture is filtered, washed with water and then dried to obtain the title product.
Workup
- filtrationThe mixture is filtered
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-d98f39d3f8ae4fa0b17e3728ef2d4618
- Source dataset
- uspto-grants-1995_02
- Patent number
- US05393775
Reaction notes
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