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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3,3,3-trifluoro-N-[(+/-)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide

HRID 10074
Notes
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Reaction equation

HRID 10074 reaction equation
[NH2:1][C@@:2]12[CH2:7][C@H:6]1[CH2:5][O:4][C:3]2=[O:8].[F:9][C:10]([F:16])([F:15])[CH2:11][C:12](O)=[O:13].OC1C2N=NNC=2C=CC=1.C(N=C=NCCCN(C)C)C>CN(C)C=O.O.C(N(CC)CC)C>[F:9][C:10]([F:16])([F:15])[CH2:11][C:12]([NH:1][C@@:2]12[CH2:7][C@H:6]1[CH2:5][O:4][C:3]2=[O:8])=[O:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 27779723,3,3-Trifluoropropionic acidHCID 21040236(+/-)-Trans-1-amino-3-oxabicyclo[3.1.0]hexan-2-oneHCID 178418300HCID 178418300, compound

Product 1

HCID 865976023,3,3-trifluoro-N-[(+/-)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamideYield 45%

Reagents, catalysts & solvents

3
HCID 962WaterSolventHCID 6228DimethylformamideSolventHCID 8471TriethylamineSolvent

Procedure

(±)-Trans-1-amino-3-oxabicyclo[3.1.0]hexan-2-one (128 mg, 1.13 mmol) was mixed with 3,3,3-trifluoropropionic acid in 2.3 mL of N,N-dimethylformamide. Hydroxybenzotriazole (17.4 mg, 0.11 mmol) was added followed by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (282 mg, 1.47 mmol). The pH of the reaction mixture was adjusted to 8.5 with triethylamine and the mixture was allowed to stir at ambient temperature for 2 hours. Water was then added and the reaction mixture was extracted with ethyl acetate. The combined organic extracts were washed with water and brine, then dried (sodium sulfate) and concentrated to give the crude product. This was purified by silica gel chromatography to afford 120 mg (45%) of 3,3,3-trifluoro-N-[(±)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide.

Workup

  1. extractionthe reaction mixture was extracted with ethyl acetate
  2. washThe combined organic extracts were washed with water and brine
  3. dry with materialdried (sodium sulfate)
  4. concentrationconcentrated
  5. customto give the crude product
  6. customThis was purified by silica gel chromatography

Sources & evidence

ORD record
ord-0300c97a88a5417abebd157852f56576
Source dataset
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07091380B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes