Sodium Hydroxide → 4-Carbamoyl-2,4,5,6-tetrahydro-1,3,4,6,6-pentamethylcyclopenta[c]pyrrole-2-acetic acid

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[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]

Komponenten

3

Versuchsvorschrift

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.

Quellen und Nachweise

ORD-Eintrag
ord-5864a8a09b8f4bf4848663672b4010d7
Quelldatensatz
uspto-grants-1978_07
Patentnummer
US04098797

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