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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 86651053, compound

HRID 1913711
Notes
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Reaction equation

HRID 1913711 reaction equation
CCN=C=NCCCN(C)C.[Cl:12][C:13]1[CH:21]=[N:20][CH:19]=[CH:18][C:14]=1[C:15]([OH:17])=O.[NH2:22][C:23]1[CH:28]=[C:27]([C:29]([F:38])([C:34]([F:37])([F:36])[F:35])[C:30]([F:33])([F:32])[F:31])[CH:26]=[CH:25][C:24]=1[OH:39]>N1C=CC=CC=1>[Cl:12][C:13]1[CH:21]=[N:20][CH:19]=[CH:18][C:14]=1[C:15]([NH:22][C:23]1[CH:28]=[C:27]([C:29]([F:38])([C:30]([F:31])([F:32])[F:33])[C:34]([F:35])([F:36])[F:37])[CH:26]=[CH:25][C:24]=1[OH:39])=[O:17]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide2×HCID 27358163-Chloropyridine-4-carboxylic acid2×HCID 866510652-Amino-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenol

Product 1

HCID 86651053HCID 86651053, compound

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

To a mixture of 0.58 g of WSC and 5 ml of pyridine 5 ml, 0.48 g of 3-chloroisonicotinic acid was added. The reaction mixture was stirred at room temperature for 25 minutes. To the reaction mixture, 0.75 g of 2-amino-4-(heptafluoroisopropyl)phenol was added and was stirred while heating at 60° C. for three hours. The reaction mixture was cooled to room temperature, the 0.24 g of 3-chloroisonicotinic acid and 0.29 g of WSC was added and stirred while heating at 60° C. for 1.5 hours and then at 80° C. for 1.3 hours. The mixture reaction was cooled to room temperature, and then concentrated under reduced pressure. Then, water was added to the residue, followed by extraction with ethyl acetate twice. The combined organic layers were washed with a saturated sodium chloride solution, was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.90 g of 3-chloro-N-[2-hydroxy-5-(heptafluoroisopropyl)phenyl]isonicotinamide.

Workup

  1. additionwas added
  2. stirringwas stirred
  3. temperaturewhile heating at 60° C. for three hours
  4. temperatureThe reaction mixture was cooled to room temperature
  5. stirringstirred
  6. temperaturewhile heating at 60° C. for 1.5 hours
  7. waitat 80° C. for 1.3 hours
  8. customThe mixture reaction
  9. temperaturewas cooled to room temperature
  10. concentrationconcentrated under reduced pressure
  11. additionThen, water was added to the residue
  12. extractionfollowed by extraction with ethyl acetate twice
  13. washThe combined organic layers were washed with a saturated sodium chloride solution
  14. dry with materialwas dried over anhydrous sodium sulfate
  15. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-1a5f2f93bb264402a534229dc3c69053
Source dataset
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08609705B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes