1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Letaxaban

HRID 2366537Notes

Reaction equation

HRID 2366537 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([S:12]([CH2:15][C@@H:16]([OH:20])[C:17]([OH:19])=O)(=[O:14])=[O:13])[CH:6]=[CH:5]2.[NH:21]1[CH2:26][CH2:25][CH:24]([N:27]2[CH2:32][CH2:31][CH2:30][NH:29][C:28]2=[O:33])[CH2:23][CH2:22]1.C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([S:12]([CH2:15][C@@H:16]([OH:20])[C:17]([N:21]1[CH2:26][CH2:25][CH:24]([N:27]3[CH2:32][CH2:31][CH2:30][NH:29][C:28]3=[O:33])[CH2:23][CH2:22]1)=[O:19])(=[O:13])=[O:14])[CH:6]=[CH:5]2

Participants

6

Procedure

(2S)-3-[(6-Chloronaphthalen-2-yl)sulfonyl]-2-hydroxypropionic acid, 1-(piperidin-4-yl)tetrahydropyrimidin-2(1H)-one, and HOBt were dissolved in DMF, WSC was added thereto, and the mixture was stirred at room temperature for 15 hours. The reaction mixture was concentrated under reduced pressure, diluted with an aqueous sodium bicarbonate solution, and extracted with dichloromethane. The extract was washed with an aqueous 5% citric acid solution and saturated saline solution, and dried over sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=10/1) to obtain the title compound as a colorless powder.

Workup

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additiondiluted with an aqueous sodium bicarbonate solution
  3. extractionextracted with dichloromethane
  4. washThe extract was washed with an aqueous 5% citric acid solution and saturated saline solution
  5. dry with materialdried over sodium sulfate
  6. distillationthe solvent was distilled off under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=10/1)

Sources & evidence

ORD record
ord-64b120ad09304fc9bc7a63417a459b58
Source dataset
uspto-grants-2014_04
Patent number
US08697865B2

Reaction notes

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