HRID868044

反应详情

EQUATION

反应方程式

HRID 868044 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

0.75 g (2.7 mmole) of 9,10-difluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid, 40 ml acetonitrile, and 0.91 g (0.80 mmole) of N-methyl-3-pyrrolidinemethanamine were refluxed overnight. The solvent was removed at reduced pressure and the residue tititrated with 40 ml of methanol. The precipitate was filtered, washed repeatedly with 95% ethanol and finally with ether until dry to give 0.68 g of 9-fluoro-2,3-dihydro-3-methyl-10-[3-[(methylamino)methyl]-1-pyrrolidinyl]-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid, mp 235°-237.5° C. Analysis for C19H22FN3O4.1/2H2O C, 59.37; H, 6.03; N, 10.93 Found C, 59.34; H, 5.78; N, 10.95.

WORKUP

后处理

  1. customThe solvent was removed at reduced pressure
  2. filtrationThe precipitate was filtered
  3. washwashed repeatedly with 95% ethanol and finally with ether
  4. customuntil dry