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N-(4-Chloro-2-methylphenyl)-N'-methylmethanimidamide → HCID 54171351, compound

HRID 1390972
Notes
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Reaction equation

HRID 1390972 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[NH:9][CH:10]=[N:11][CH3:12].C(O[CH:16]=[N:17][S:18]([CH3:21])(=[O:20])=[O:19])C>O1CCOCC1>[CH3:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[N:9]=[CH:10][N:11]([CH3:12])[CH:16]=[N:17][S:18]([CH3:21])(=[O:19])=[O:20]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 30814N-(4-Chloro-2-methylphenyl)-N'-methylmethanimidamideHCID 54392285Ethyl (methanesulfonyl)methanimidate

Product 1

HCID 54171351HCID 54171351, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Conditions

Temperature
60 °C

Procedure

To a solution of 18.2 g of N-(2-methyl-4-chlorophenyl)-N'-methylformamidine in 60 ml of abs. dioxane are added dropwise at room temperature 15.1 g of N-ethoxymethylenemethanesulphonamide and the solution is stirred for 1 hour at 60° C. The reaction mixture is subsequently concentrated and the crystallised product is recrystallised from toluene, affording the compound of the formula ##STR4## as a white powder with a melting point of 142°-143° C. The following compounds are also prepared in analogous manner: ##STR5##

Workup

  1. concentrationThe reaction mixture is subsequently concentrated
  2. customthe crystallised product is recrystallised from toluene
  3. customaffording the compound of the formula ##STR4## as a white powder with a melting point of 142°-143° C
  4. customThe following compounds are also prepared in analogous manner

Sources & evidence

ORD record
ord-906542eee45f47468fb2c2d1c86bbd1e
Source dataset
uspto-grants-1979_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04140795

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes