1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 86603732, compound

HRID 2376122Notes

Reaction equation

HRID 2376122 reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][C@@H:10]([NH:13][C:14]2[N:19]=[CH:18][C:17](/[CH:20]=[CH:21]/[C:22]([OH:24])=O)=[CH:16][CH:15]=2)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C1C=CC2[N:33]([OH:34])N=NC=2C=1.CCN=C=N[CH2:40][CH2:41][CH2:42]N(C)C.[C:46](OCC)([CH3:48])=[O:47].O>CN(C=O)C>[O:24]=[C:22]([NH:33][O:34][CH:40]1[CH2:41][CH2:42][CH2:48][CH2:46][O:47]1)/[CH:21]=[CH:20]/[C:17]1[CH:16]=[CH:15][C:14]([NH:13][C@@H:10]2[CH2:11][CH2:12][N:8]([C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7])[CH2:9]2)=[N:19][CH:18]=1

Participants

6

Reactant 4

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 22728543Water ethylacetateHCID 68962851HCID 68962851, compound

Product 1

HCID 86603732HCID 86603732, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

A mixture of (2E)-3-(6-{[(3R)-1-(tert-butoxycarbonyl)-3-pyrrolidinyl]amino}-3-pyridinyl)acrylic acid (450 mg), 0-(tetrahydro-2H-pyran-2-yl)hydroxylamine (174 mg), HOBt (191 mg) and EDCI (220 mg) in DMF (20 ml) was stirred at ambient temperature for 15 hours. The reaction mixture was poured into a mixture of AcOEt-H2O and the organic layer was washed with brine and dried over MgSO4. The solvent was evaporated in vacuo and the residue was chromatographed on silicagel eluting with AcOEt-MeOH (95:5). The eluted fractions containing the desired product were collected and evaporated in vacuo to give tert-butyl (3R)-3-[(5-[(1E)-3-oxo-3-[(tetrahydro-2H-pyran-2-yloxy)amino]-1-propen-1-yl)-2-pyridinyl)amino]-1-pyrrolidinecarboxylate (450 mg).

Workup

  1. washthe organic layer was washed with brine
  2. dry with materialdried over MgSO4
  3. customThe solvent was evaporated in vacuo
  4. customthe residue was chromatographed on silicagel
  5. washeluting with AcOEt-MeOH (95:5)
  6. additionThe eluted fractions containing the desired product
  7. customwere collected
  8. customevaporated in vacuo

Sources & evidence

ORD record
ord-1cb4c2f3c53542e0a6751374b15f7efd
Source dataset
uspto-grants-2008_12
Patent number
US07465731B2

Reaction notes

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