Ethanol → HCID 21896917, compound

HRID 1375521Notes

Reaction equation

HRID 1375521 reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[C:11]([Cl:17])[CH:10]=2)[N:5]=[C:4]([NH:18][CH:19]2[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)[N:3]=1.C([O-])([O-])=O.[K+].[K+].[CH2:32]([OH:34])[CH3:33]>>[CH2:32]([O:34][C:2]1[N:7]=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[C:11]([Cl:17])[CH:10]=2)[N:5]=[C:4]([NH:18][CH:19]2[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)[N:3]=1)[CH3:33]

Participants

4

Reactant 3

HCID 702EthanolHCID 11430Potassium CarbonateHCID 218970216-chloro-N-(3-chloro-4-methoxyphenyl)-N'-cycloheptyl-[1,3,5]triazine-2,4-diamine

Product 1

HCID 21896917HCID 21896917, compound

Procedure

A portion of 6-chloro-N-(3-chloro-4-methoxyphenyl)-N′-cycloheptyl-[1,3,5] triazine-2,4-diamine (5 g) was refluxed in ethanol in presence of K2CO3 (3.2g) for about 8–10 h. TLC was monitored. After the completion of the reaction, the reaction mass was filtered through vacuum and the filtrate was evaporated to yield the title compound. (Wt. 4.6 g Y: 90%).

Workup

  1. customAfter the completion of the reaction
  2. filtrationthe reaction mass was filtered through vacuum
  3. customthe filtrate was evaporated

Sources & evidence

ORD record
ord-ded45a8fb47a45218dae14b29a1bb3f9
Source dataset
uspto-grants-2007_01
Patent number
US07169785B2

Reaction notes

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