Dimethylamine → HCID 67586773, compound

HRID 611310Notes

Reaction equation

HRID 611310 reaction equation
Cl.[O:2]1[C:6]2[CH2:7][NH:8][CH2:9][CH2:10][C:5]=2[CH:4]=[CH:3]1.[Cl:11][C:12]1[CH:17]=[CH:16][C:15](/[CH:18]=[CH:19]\[C:20]2[CH:25]=[CH:24][C:23]([C:26]([OH:28])=O)=[CH:22][CH:21]=2)=[CH:14][CH:13]=1.[CH2:29]([N:31]([CH2:34]C)[CH2:32]C)C.C(P(=O)(OCC)OCC)#N.CNC.C=O>ClCCl>[ClH:11].[CH3:29][N:31]([CH2:34][C:3]1[O:2][C:6]2[CH2:7][N:8]([C:26]([C:23]3[CH:24]=[CH:25][C:20](/[CH:19]=[CH:18]\[C:15]4[CH:16]=[CH:17][C:12]([Cl:11])=[CH:13][CH:14]=4)=[CH:21][CH:22]=3)=[O:28])[CH2:9][CH2:10][C:5]=2[CH:4]=1)[CH3:32]

Participants

8

Reactant 6

HCID 674DimethylamineHCID 712FormaldehydeHCID 8471TriethylamineHCID 76257Diethyl cyanophosphonateHCID 195999074,5,6,7-Tetrahydrofuro[2,3-c]pyridine hydrochlorideHCID 69554542HCID 69554542, compound

Product 1

HCID 67586773HCID 67586773, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 0.319 g (2.000 mmol) of 4,5,6,7-tetrahydrofuro[2,3-c]pyridine hydrochloride, 0.569 g (2.2 mmol) of (Z)-4-chlorostilbene-4'-carboxylic acid and 1.1 ml (8.0 mmol) of triethylamine in 30 ml of dichloromethane, 0.489 g (3.0 mmol) of diethyl cyanophosphonate was added dropwise at room temperature, followed by overnight stirring at room temperature. After the solvent was distilled off, water was added, followed by 2 extractions with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was dissolved in 10 ml of acetic acid; 0.270 ml (3.00 mmol) of 50% aqueous dimethylamine and 0.245 ml (3.00 mmol) of 37% aqueous formaldehyde were added, followed by stirring at 100° C. for 120 minutes. After the solvent was distilled off under reduced pressure, the residual solution was alkalified with 5% aqueous sodium hydrogen carbonate and extracted with ethyl acetate 2 times. The combined organic layer was washed with water and dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (ethyl acetate/methanol=5/1) to yield the desired product.

Workup

  1. distillationAfter the solvent was distilled off
  2. additionwater was added
  3. extractionfollowed by 2 extractions with ethyl acetate
  4. dry with materialThe combined organic layer was dried over anhydrous sodium sulfate
  5. distillationthe solvent was distilled off under reduced pressure
  6. dissolutionThe resulting crude product was dissolved in 10 ml of acetic acid
  7. stirringby stirring at 100° C. for 120 minutes
  8. distillationAfter the solvent was distilled off under reduced pressure
  9. extractionextracted with ethyl acetate 2 times
  10. washThe combined organic layer was washed with water
  11. dry with materialdried over anhydrous sodium sulfate
  12. distillationthe solvent was distilled off under reduced pressure
  13. customThe resulting crude product was purified by silica gel column chromatography (ethyl acetate/methanol=5/1)

Sources & evidence

ORD record
ord-f0a5099158004fa2b6aba3359677fef2
Source dataset
uspto-grants-1999_12
Patent number
US05998433

Reaction notes

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