Water → 2-(Chloromethyl)-N-[6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazol-4-yl]-1,3-thiazole-4-carboxamide

Temperatur

0 °C

To solution of 6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazol-4-amine (1.5 g, 3.86 mmol) in chloroform (20 ml) at 0° C. was added DIPEA (1.35 ml, 7.72 mmol). 2-(Chloromethyl)-1,3-thiazole-4-carbonyl chloride (1.8 g, 6.98 mmol) in chloroform (20 ml) was added dropwise and the mixture was stirred at 0° C. for 1 h 15 mins. The mixture was allowed to warm to room temperature and stirring continued for 18 h. A further portion of 2-(chloromethyl)-1,3-thiazole-4-carbonyl chloride (0.2 g, 1.02 mmol) was added to the mixture which was stirred at room temperature for 30 mins. Water (50 ml) was added to quench the reaction and the mixture was extracted with DCM (2×100 ml), separating the layers using a hydrophobic frit. The organics were collected and solvent removed in vacuo to give a brown solid which was triturated with ether (10 ml). The solid was filtered off and dried in a vacuum oven overnight to afford the title compound (1.6 g).

1. temperatureto warm to room temperature
2. stirringstirring
3. waitcontinued for 18 h
4. stirringwas stirred at room temperature for 30 mins
5. customto quench
6. customthe reaction
7. extractionthe mixture was extracted with DCM (2×100 ml)
8. customseparating the layers
9. customThe organics were collected
10. customsolvent removed in vacuo
11. customto give a brown solid which
12. customwas triturated with ether (10 ml)
13. filtrationThe solid was filtered off
14. customdried in a vacuum oven overnight

ORD-Eintrag

ord-7284d3b6ef9a4bcbafa4616bbda56ee6

Quelldatensatz

uspto-grants-2014_02

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08658635B2