Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

C12H10Cl2N4O synthesis

6synthesis methods
5750-76-5 Synthesis
2,4,5-Trichloropyrimidine

5750-76-5
352 suppliers
$5.00/1g

4141-08-6 Synthesis
2-AMINO-N-METHYLBENZAMIDE

4141-08-6
132 suppliers
$14.00/1g

C12H10Cl2N4O

761440-08-8
21 suppliers
inquiry

-

Yield:761440-08-8 95%

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine in isopropyl alcohol; for 18 h;Heating / reflux;

Steps:

2

Intermediate 2; 2-[(2,5-Dichloro-4-pyrimidinyl)amino]-N-methylbenzamide A round-bottomed flask was charged with 2,4,5-trichloropyrimidine (2 g, 11.1 mmol), 2-amino-N-methylbenzamide (2 g, 13.3 mmol), di-isopropyl-ethylamine (2.3 mL, 13.3 mmol) and 40 mL isopropanol. The flask was fitted with a reflux condenser and the reaction was heated to reflux and stirred for 18 h. A white solid appeared in the reaction mixture. The reaction was cooled to room temperature, and the solid was filtered off and washed with isopropanol. After drying, the white solid (3.16 g, 10.5 mmol, 95% yield) was identified as 2-[(2,5-dichloro-4-pyrimidinyl)amino]-N-methylbenzamide. MS: M(C12H10Cl2N4O)=297.14, (M+H)+=297 and 299.

References:

US2008/182852,2008,A1 Location in patent:Page/Page column 7-8