تفاعل #47310

ord-b4698883b4c94615acdc4ffcd0a8dce0

معادلة التفاعل

CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
CC(C)(C)OC(=O)N[C@@H](CC1CCCCO1)C(=O)O
(S)-2-t-butoxycarbonylamino-3-(tetrahydro-pyran-2-yl)-propionic acid
CC(C)C[C@@H](C(=O)Nc1ccn(C[C@@H](O)CO)n1)N1CC(Oc2cccc(Cl)c2Cl)=CC1=O.Cl
1-(3-amino-pyrazol-1-yl)-2-methyl-propan-2-ol
CC(C)C[C@@H](C(=O)Nc1ccn(C[C@@H](O)CO)n1)N1CC(Oc2cccc(Cl)c2Cl)=CC1=O.Cl
(S)-2-[4-(2,3-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid [1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-amide hydrochloride
CN(C)[P+](On1nnc2ccccc21)(N(C)C)N(C)C.F[P-](F)(F)(F)(F)F
benzotriazol-1-yl-oxy-tris(dimethylamino)phosphonium hexafluorophosphate
CC(C)(O)Cn1ccc(NC(=O)[C@H](CC2CCCCO2)NC(=O)OC(C)(C)C)n1
[(S)-1-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-ylcarbamoyl]-2-(tetrahydro-pyran-2-yl)-ethyl]-carbamic acid t-butyl ester
المردود 57.1%

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe mixture was stirred at room temperature overnight
  2. 2
    أخرىsolvents were evaporated
  3. 3
    workup.ADDITIONThe residue was treated with ethyl acetate and ammonium chloride solution
  4. 4
    أخرىthe organic layer separated
  5. 5
    غسيلThe organic layer was washed with saturated sodium chloride solution
  6. 6
    تجفيفdried over sodium sulfate
  7. 7
    أخرىSolvents were evaporated
  8. 8
    أخرىthe residue was purified through flash column chromatography (silica gel, 5 to 100% ethyl acetate/hexanes)

الإجراء التجريبي

To a solution of (S)-2-t-butoxycarbonylamino-3-(tetrahydro-pyran-2-yl)-propionic acid (700 mg, 2.56 mmol) in N,N-dimethylformamide (6 mL) was added 1-(3-amino-pyrazol-1-yl)-2-methyl-propan-2-ol (prepared in U.S. Pat. Appl. US2008021032 Example 80, 398 mg, 2.57 mmol) and benzotriazol-1-yl-oxy-tris(dimethylamino)phosphonium hexafluorophosphate (1.36 g, 3.0 mmol). The mixture was stirred at 0° C. and N,N-diisopropylethylamine (0.4 mL) was added. The mixture was stirred at room temperature overnight and solvents were evaporated. The residue was treated with ethyl acetate and ammonium chloride solution, and the organic layer separated. The organic layer was washed with saturated sodium chloride solution and dried over sodium sulfate. Solvents were evaporated and the residue was purified through flash column chromatography (silica gel, 5 to 100% ethyl acetate/hexanes) to afford [(S)-1-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-ylcarbamoyl]-2-(tetrahydro-pyran-2-yl)-ethyl]-carbamic acid t-butyl ester (600 mg, 57%) as a white solid: LR-ES-MS m/z calculated for C20H34N4O5 [M]+ 410, observed [M+H]+ 411.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07741327B2uspto-grants-2010_06