1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 57008919, compound

HRID 1088611Notes

Reaction equation

HRID 1088611 reaction equation
S([NH:11][C@H](C(O)=O)CC1N=CNC=1)(C1C=CC(C)=CC=1)(=O)=O.N[C@H:23]([C@@H:31]([OH:37])[CH2:32][CH2:33][CH:34]([CH3:36])[CH3:35])[CH2:24][CH:25]1[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]1.C(N=C=NCCCN(C)C)C>C(Cl)Cl>[NH2:11][CH:24]([CH:25]1[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]1)[CH2:23][C@@H:31]([OH:37])[CH2:32][CH2:33][CH:34]([CH3:36])[CH3:35]

Participants

5

Procedure

To a solution of Nα -t-butoxycarbonyl-Nα -methyl-Nim -tosyl-L-histidine (2.77 g) and 2(S)-amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (1.49 g) in dry methylene chloride (60 ml) which was cooled at 0° C., was added N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide (1.25 g). The mixture was stirred at ambient temperature for 3 hours. After evaporation of the solvent, the residue was dissolved in ethyl acetate (200 ml) and the solution was washed with 0.5% hydrochloric acid, saturated sodium bicarbonate solution and water successively, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (1% methanol in chloroform as eluent) to give 2(S)-(Nα -t-butoxycarbonyl-Nα -methyl-Nim -tosyl-L-histidyl)amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (1.61 g) as an amorphous powder.

Workup

  1. customAfter evaporation of the solvent
  2. dissolutionthe residue was dissolved in ethyl acetate (200 ml)
  3. washthe solution was washed with 0.5% hydrochloric acid, saturated sodium bicarbonate solution and water successively
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified with silica gel column chromatography (1% methanol in chloroform as eluent)

Sources & evidence

ORD record
ord-25232ec04c2c4868a50781911779f46c
Source dataset
uspto-grants-1990_10
Patent number
US04963530

Reaction notes

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