반응 #43275

ord-6d934af18b0a4f2baa267241da828b8e

반응 방정식

O=C(O)C(CC1CCOCC1)c1ccc2c(c1)Nc1ccccc1S2(=O)=O
2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-(tetrahydropyran-4-yl)propionic acid
Cn1ccc(N)n1
1-methyl-1H-pyrazole-3-amine
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
On1nnc2cccnc21
HOAT
Cn1ccc(NC(=O)C(CC2CCOCC2)c2ccc3c(c2)Nc2ccccc2S3(=O)=O)n1
2-(5,5-Dioxo-5,10-dihydrophenothiazin-2-yl)-N-(1-methyl-1H-pyrazol-3-yl)-3-(tetrahydropyran-4-yl)propionamide

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed three times with in each case 50 ml of water and saturated sodium chloride solution
  2. 2
    건조The organic phase is dried over MgSO4
  3. 3
    기타the solvent is then removed under reduced pressure
  4. 4
    기타The residue is purified by RP-HPLC

실험 절차

600 mg of 2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-(tetrahydropyran-4-yl)propionic acid, 120 mg of commercially available 1-methyl-1H-pyrazole-3-amine and 729 μl of N,N-diisopropylethylamine are dissolved in 5 ml of dimethylformamide. 561 mg of HATU and 200 mg of HOAT are added, and the mixture is stirred at room temperature for two hours. The reaction mixture is then diluted by addition of 200 ml of ethyl acetate and washed three times with in each case 50 ml of water and saturated sodium chloride solution. The organic phase is dried over MgSO4, and the solvent is then removed under reduced pressure. The residue is purified by RP-HPLC. This gives 200 mg of 2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(11-methyl-1H-pyrazol-3-yl)-3-(tetrahydropyran-4-yl)propionamide as a colorless lyophilisate.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07732440B2uspto-grants-2010_06