HCID 57294807, compound → HCID 57083083, compound

HRID 1413057Notes

Reaction equation

HRID 1413057 reaction equation
[CH3:1][N:2]1[C:6](=[N:7][CH:8]([Cl:11])[CH2:9][Cl:10])[C:5](=[O:12])[N:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2Cl)[C:3]1=[O:20].[Cl:21][C:22]1C=[CH:26][CH:25]=[CH:24][C:23]=1N1C(=NC(Cl)CCl)CN(C)C1>>[Cl:21][C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][C:1]=1[N:2]1[C:6](=[N:7][CH:8]([Cl:11])[CH2:9][Cl:10])[C:5](=[O:12])[N:4]([CH:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]2)[C:3]1=[O:20]

Participants

3

Reactant 2

HCID 57294807HCID 57294807, compoundHCID 86737463HCID 86737463, compound

Product 1

HCID 57083083HCID 57083083, compound

Procedure

Similarly the reverse 1-position-3-position isomers of each of the above prepared compounds are prepared by using the corresponding position isomer of formula A as the starting material. For example, by using 1-methyl-3-(2-chlorophenyl)-5-(1,2-dichloroethyl)imino-1,3-diazolidine-2,4-dione in place of 1-(2-chlorophenyl-3-methyl-5-(1,2-dichloroethyl)imino-1,3-diazolidine the following compounds (as well as the other 1-3 positions isomers of each of the above products are prepared:

Workup

  1. customSimilarly the reverse 1-position-3-position isomers of each of the above prepared compounds are prepared
  2. customare prepared

Sources & evidence

ORD record
ord-ba1c3f38927e41da988af956e4dd1492
Source dataset
uspto-grants-1981_02
Patent number
US04248620

Reaction notes

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