Sodium Hydroxide → 4-Carbamoyl-2,4,5,6-tetrahydro-1,3,4,6,6-pentamethylcyclopenta[c]pyrrole-2-acetic acid
反応式
[C:1]([C:4]1([CH3:22])[C:11]2[C:7](=[C:8]([CH3:19])[N:9]([CH2:13][C:14]([O:16]CC)=[O:15])[C:10]=2[CH3:12])[C:6]([CH3:21])([CH3:20])[CH2:5]1)(=[O:3])[NH2:2].[OH-].[Na+]>>[C:1]([C:4]1([CH3:22])[C:11]2[C:7](=[C:8]([CH3:19])[N:9]([CH2:13][C:14]([OH:16])=[O:15])[C:10]=2[CH3:12])[C:6]([CH3:21])([CH3:20])[CH2:5]1)(=[O:3])[NH2:2]参加物
3
実験手順
Reaction of the ethyl 4-carbamoyl-2,4,5,6-tetrahydro-1,3,4,6,6-pentamethylcyclopenta[c]pyrrole-2-acetate described above in Example 20AC with alcoholic sodium hydroxide and isolation of the product from an acid or neutral medium affords 4-carbamoyl-2,4,5,6-tetrahydro-1,3,4,6,6-pentamethylcyclopenta[c]pyrrole-2-acetic acid.
出典と根拠
- ORDレコード
- ord-3d47786f72884d77b0cf6cb99bc5d5c7
- 出典データセット
- uspto-grants-1979_02