Trifluoroacetic acid → Methyl 2-[[(1,1'-biphenyl)-4-yl]sulfonyl]amino-4-pentenoate

HRID 413365Notes

Reaction equation

HRID 413365 reaction equation
[CH3:1][O:2][C:3](=[O:16])[CH2:4][N:5](CC=C)C(OC(C)(C)C)=O.F[C:18](F)(F)[C:19](O)=O.[CH2:24](N(CC)CC)C.[C:31]1([C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)[CH:36]=[CH:35][C:34]([S:37](Cl)(=[O:39])=[O:38])=[CH:33][CH:32]=1>C(Cl)Cl.O>[C:31]1([C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)[CH:36]=[CH:35][C:34]([S:37]([NH:5][CH:4]([CH2:24][CH:18]=[CH2:19])[C:3]([O:2][CH3:1])=[O:16])(=[O:39])=[O:38])=[CH:33][CH:32]=1

Participants

7

Procedure

To a solution of N-Boc-allylglycine methyl ester 1a (4.0 g, 17.6 mmol) in CH2Cl2 (15 mL is added trifluoroacetic acid (10 mL) slowly, and the resulting mixture is stirred overnight at room temperature. The reaction mixture is concentrated under reduced pressure to dryness then dissolved in dioxane (15 mL) and water (15 mL). To the solution is added triethyl amine (9.8 mL, 70.4 mmol), followed by biphenyl-4-sulfonyl chloride (5.9 g, 21.12 mmol) and the mixture is stirred overnight. The reaction mixture is diluted with water, extracted three times with EtOAc. The combined EtOAc layer is washed with 1 N HCl, H2O, brine, dried, and concentrated to an oil which solidified upon standing. The crude product is recrystallized from EtOAc/hexane to give the desired product.

Workup

  1. concentrationThe reaction mixture is concentrated under reduced pressure to dryness
  2. dissolutionthen dissolved in dioxane (15 mL)
  3. stirringthe mixture is stirred overnight
  4. extractionextracted three times with EtOAc
  5. washThe combined EtOAc layer is washed with 1 N HCl, H2O, brine
  6. customdried
  7. concentrationconcentrated to an oil which
  8. customThe crude product is recrystallized from EtOAc/hexane

Sources & evidence

ORD record
ord-b0f99f7f01f242c099f9b102c92941f9
Source dataset
uspto-grants-2003_05
Patent number
US06566381B1

Reaction notes

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