成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

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!

ChemicalBook CAS DataBase List Erlotinib iMpurity 2
299912-59-7

Erlotinib iMpurity 2 synthesis

7synthesis methods
-

Yield:299912-59-7 100%

Reaction Conditions:

in acetonitrile at 25; for 5 h;Inert atmosphere;Reflux;

Steps:

9

Example 9 - Synthesis of 3-Butyn-2-ol, 4-[3-[[6,7-bis(2-methoxyethoxy)-4-quinazolinyl]amine] phenyl]-2-methyl-, hydrochloride (1:1) of formula (II) - exemplifying the invention.; Synthesis scheme [Show Image] In a 500 ml flask provided with a thermometer there are introduced - in succession at 25°C and under nitrogen atmosphere - 1 5 g of 4-chloro-6,7-bis(2-methoxyethoxy)quinazoline of formula (III), 9.2 g of 4-(3-aminophenyl)-2-methyl-3-butyn-2-ol of formula (IV) and 225 mL of Acetonitrile. The mixture is heated at reflux for 5 hours. Upon completing the reaction the mixture is cooled to 0-5°C and maintained at that temperature under stirring for at least 1 hour. The suspension is filtered and the solid is washed using 15 mL of cold Acetonitrile. The product is dried under vacuum for at least 8 hours obtaining 23.4 g of product as a white solid for a molar yield equivalent to 100%.

References:

EP2433931,2012,A1 Location in patent:Page/Page column 11

Erlotinib iMpurity 2 Related Search: