Triethylamine → HCID 67696610, compound

HRID 611145Notes

Reaction equation

HRID 611145 reaction equation
Cl.[O:2]1[C:10]2[CH2:9][CH2:8][NH:7][CH2:6][C:5]=2[CH:4]=[CH:3]1.[O:11]=[C:12]1[C:25]2[CH:24]=[CH:23][C:22]([C:26](O)=[O:27])=[CH:21][C:20]=2[S:19](=[O:30])(=[O:29])[C:18]2[C:13]1=[CH:14][CH:15]=[CH:16][CH:17]=2.C(N(CC)CC)C.C(P(=O)(OCC)OCC)#N>ClCCl.O>[O:11]=[C:12]1[C:25]2[CH:24]=[CH:23][C:22]([C:26]([N:7]3[CH2:8][CH2:9][C:10]4[O:2][CH:3]=[CH:4][C:5]=4[CH2:6]3)=[O:27])=[CH:21][C:20]=2[S:19](=[O:30])(=[O:29])[C:18]2[C:13]1=[CH:14][CH:15]=[CH:16][CH:17]=2

Participants

7

Reactant 4

HCID 8471TriethylamineHCID 401183-Carboxy-thioxanthone-10,10-dioxideHCID 76257Diethyl cyanophosphonateHCID 195999414,5,6,7-Tetrahydrofuro[3,2-c]pyridine hydrochloride

Product 1

HCID 67696610HCID 67696610, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6344DichloromethaneSolvent

Procedure

To a solution of 0.160 g (1.000 mmol) of 4,5,6,7-tetrahydrofuro[3,2-c]pyridine hydrochloride, 0.346 g (1.2 mmol) of 9-oxo-9H-thioxanthene-3-carboxylic acid 10,10-dioxide and 0.55 ml (4.0 mmol) of triethylamine in 30 ml of dichloromethane, 0.24 g (1.5 mmol) of diethyl cyanophosphonate was added under ice-cooling, followed by overnight stirring at room temperature. The reaction mixture was poured into water and extracted with dichloromethane 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 (hexane/ethyl acetate=1/1) to yield the desired product.

Workup

  1. temperaturecooling
  2. extractionextracted with dichloromethane 2 times
  3. washThe combined organic layer was washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationthe solvent was distilled off under reduced pressure
  6. customThe resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate=1/1)

Sources & evidence

ORD record
ord-60e8752e5c434a83a40b399d1d8c71d2
Source dataset
uspto-grants-1999_12
Patent number
US05998433

Reaction notes

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