HCID 57143475, compound → HCID 57145422, compound

HRID 1413059Notes

Reaction equation

HRID 1413059 reaction equation
[CH3:1][N:2]1[C:6](=[N:7][CH:8]([Cl:15])[CH:9]([Cl:14])[C:10]([Cl:13])([Cl:12])[Cl:11])[C:5](=[O:16])[N:4]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2F)[C:3]1=[O:24].[F:25][C:26]1C=[CH:30][CH:29]=[CH:28][C:27]=1N1C(=NC(Cl)C(Cl)C(Cl)(Cl)Cl)CN(C)C1>>[F:25][C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][C:1]=1[N:2]1[C:6](=[N:7][CH:8]([Cl:15])[CH:9]([Cl:14])[C:10]([Cl:12])([Cl:11])[Cl:13])[C:5](=[O:16])[N:4]([CH:17]2[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]2)[C:3]1=[O:24]

Participants

3

Reactant 2

HCID 57143475HCID 57143475, compoundHCID 86737464HCID 86737464, compound

Product 1

HCID 57145422HCID 57145422, 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-fluorophenyl)-5-(1,2,3,3,3-pentachloropropyl)imino-1,3-diazolidine-2,4-dione in place of 1-(2-fluorophenyl-3-methyl-5-(1,2,3,3,3-pentachloropropyl)imino-1,3-diazolidine the following compounds (as well as the other position isomers 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-4bfb84d40bba49d1a7442b4005f6faf0
Source dataset
uspto-grants-1981_02
Patent number
US04248620

Reaction notes

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