Reaktion #619171

ord-f2b37b32cf4a43bbaef0beff700799dd

Reaktionsgleichung

CCN(C(C)C)C(C)C
DIEA
O=C(O)c1cnc(NC(=O)N(C2CCCCC2)C2CCCCC2)s1
2-(3,3-Dicyclohexyl-ureido)-thiazole-5-carboxylic acid
CN(C)S(=O)(=O)N1CCNCC1.Cl
piperazine sulfonic acid dimethylamide hydrochloride
CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HBTU
CN(C)S(=O)(=O)N1CCN(C(=O)c2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
desired compound
Ausbeute 67.1%
CN(C)S(=O)(=O)N1CCN(C(=O)c2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
4-[2-(3,3-Dicyclohexyl-ureido)-thiazole-5-carbonyl]-piperazine-1-sulfonic acid dimethylamide
Ausbeute 67.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONadded to a 10 mL reaction flask
  2. 2
    Sonstigequenched with saturated aqueous NH4Cl (5 mL)
  3. 3
    SonstigeAfter separation and extraction with EtOAc (2×5 mL) the combined organic portions
  4. 4
    Trocknenwere dried over MgSO4
  5. 5
    SonstigePurification with silica gel (10% EtOAc and 1% MeOH in CH2Cl2)

Vorschrift

2-(3,3-Dicyclohexyl-ureido)-thiazole-5-carboxylic acid (53 mg, 0.15 mmol), piperazine sulfonic acid dimethylamide hydrochloride (44 mg, 0.19 mmol), and HBTU (74 mg, 0.19 mmol) were weighed out and added to a 10 mL reaction flask. DMF (1.5 mL) and DIEA (65 μL, 0.38 mmol) were added. The reaction was stirred under nitrogen at ambient temperature overnight. The reaction was diluted with EtOAc (5 mL) and quenched with saturated aqueous NH4Cl (5 mL). After separation and extraction with EtOAc (2×5 mL) the combined organic portions were dried over MgSO4. Purification with silica gel (10% EtOAc and 1% MeOH in CH2Cl2) afforded 53 mg (67%) of the desired compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE045183E1uspto-grants-2014_10