Dimethylformamide → HCID 178513110, compound

HRID 1021319Notes

Reaction equation

HRID 1021319 reaction equation
[F:1][C:2]1[C:7]([CH2:8][OH:9])=[CH:6][CH:5]=[CH:4][C:3]=1[N:10]1[CH2:15][CH2:14][C:13]([C:17]2[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=2)([OH:16])[CH2:12][CH2:11]1.C[N:24](C=O)C.C1N=CN([C:33]([N:35]2[CH:39]=[N:38]C=C2)=[O:34])C=1.C(=O)(O)O.NC(N)=N>O>[C:39]([NH:35][C:33](=[O:34])[O:9][CH2:8][C:7]1[CH:6]=[CH:5][CH:4]=[C:3]([N:10]2[CH2:11][CH2:12][C:13]([OH:16])([C:17]3[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=3)[CH2:14][CH2:15]2)[C:2]=1[F:1])(=[NH:38])[NH2:24]

Participants

6

Procedure

1-[2-Fluoro-3-(hydroxymethyl)phenyl]-4-(pyridin-3-yl)piperidin-4-ol (187 mg), DMF (5.5 ml), and CDI (201 mg) were mixed, followed by stirring at room temperature for 2 hours. Guanidine carbonate (279 mg) was added to the reaction mixture, followed by stirring at room temperature overnight. Water was added to the reaction mixture, followed by ice-cooling and stirring for 30 minutes, and the generated solid was collected by filtration, washed with water, and then dried at 50° C. under reduced pressure. The obtained solid was purified by silica gel column chromatography (CHCl3/MeOH) to obtain 2-fluoro-3-[4-hydroxy-4-(pyridin-3-yl)piperidin-1-yl]benzyl carbamimidoylcarbamate (160 mg).

Workup

  1. stirringby stirring at room temperature overnight
  2. temperaturecooling
  3. stirringstirring for 30 minutes
  4. filtrationthe generated solid was collected by filtration
  5. washwashed with water
  6. customdried at 50° C. under reduced pressure
  7. customThe obtained solid was purified by silica gel column chromatography (CHCl3/MeOH)

Sources & evidence

ORD record
ord-c0167c85fa5241aeaefa3f2ab7cd1a7f
Source dataset
uspto-grants-2014_05
Patent number
US08716470B2

Reaction notes

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