Sodium hydride → N-[4-[(4-cyanophenyl)amino]-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]-N'-(1-methylethyl)urea

HRID 843637Notes

Reaction equation

HRID 843637 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([CH2:8][C:9]2[C:14]([Cl:15])=[CH:13][CH:12]=[CH:11][C:10]=2[Cl:16])[N:5]=[C:4]([NH:17][C:18]2[CH:25]=[CH:24][C:21]([C:22]#[N:23])=[CH:20][CH:19]=2)[N:3]=1.[H-].[Na+].[N:28]([CH:31]([CH3:33])[CH3:32])=[C:29]=[O:30]>CN(C=O)C>[C:22]([C:21]1[CH:20]=[CH:19][C:18]([NH:17][C:4]2[N:5]=[C:6]([CH2:8][C:9]3[C:14]([Cl:15])=[CH:13][CH:12]=[CH:11][C:10]=3[Cl:16])[N:7]=[C:2]([NH:1][C:29]([NH:28][CH:31]([CH3:33])[CH3:32])=[O:30])[N:3]=2)=[CH:25][CH:24]=1)#[N:23]

Participants

5

Procedure

A mixture of compound (1) (1.0 g) and sodium hydride (0.11 g), in DMF (20 ml) was stirred for 20 minutes at RT under argon flow. Then, 2-isocyanato-propane (0.27 ml) was added dropwise over 30 minutes and the reaction mixture was allowed to stir at RT overnight. The solvent was evaporated and water added. The residue was filtered, washed with water and diethyl ether, and recrystallized from 1,4-dioxane. The precipitate was filtered off and dried, yielding 0.95 g (85.1 %) of N-[4-[(4-cyanophenyl)amino]-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]-N′-(1-methylethyl)urea (compound 6, mp. 267-268° C.).

Workup

  1. customThe solvent was evaporated
  2. additionwater added
  3. filtrationThe residue was filtered
  4. washwashed with water and diethyl ether
  5. customrecrystallized from 1,4-dioxane
  6. filtrationThe precipitate was filtered off
  7. customdried

Sources & evidence

ORD record
ord-40fcf192cfb9406f89becab77e995ce9
Source dataset
uspto-grants-2002_04
Patent number
US06380194B1

Reaction notes

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