HCID 24765764, compound → HCID 57422601, compound

HRID 1097270Notes

Reaction equation

HRID 1097270 reaction equation
[CH3:1][N:2]1[C:7](=[O:8])[C:6]([CH3:24])([N:9]2[C:17](=[O:18])[C:16]3[C:11](=[C:12]([F:22])[C:13]([F:21])=[C:14]([F:20])[C:15]=3[F:19])[C:10]2=[O:23])[C:5](=[O:25])[NH:4][C:3]1=[O:26].Cl.N[C:29]1(C)C(=O)N(CCC)C(=O)N[C:30]1=O>>[CH3:24][C:6]1([N:9]2[C:17](=[O:18])[C:16]3[C:11](=[C:12]([F:22])[C:13]([F:21])=[C:14]([F:20])[C:15]=3[F:19])[C:10]2=[O:23])[C:7](=[O:8])[N:2]([CH2:1][CH2:29][CH3:30])[C:3](=[O:26])[NH:4][C:5]1=[O:25]

Participants

3

Reactant 2

HCID 24765764HCID 24765764, compoundHCID 66810716HCID 66810716, compound

Product 1

HCID 57422601HCID 57422601, compound

Procedure

Compound 19b was synthesized in the same manner as described for 19a from 5-amino-5-methyl-1-propylbarbituric acid hydrochloride (0.38 g, 1.50 mmol). The crude product was recrystallized from EtOH (70%) to give 5-methyl-1-propyl-5-(tetrafluorophthalimido)-barbituric acid (19b) as white solid.

Workup

  1. customCompound 19b was synthesized in the same manner
  2. customThe crude product was recrystallized from EtOH (70%)

Sources & evidence

ORD record
ord-9b978279087f48598c554d2f149396ef
Source dataset
uspto-grants-2012_03
Patent number
US08143252B2

Reaction notes

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