反应 #1869196

ord-ccf3fbfdecfa45b4b7a9b1ffc953c189

反应方程式

CCOC(=O)CS
ethyl 2-mercaptoacetate
[H-].[Na+]
sodium hydride
COC(=O)c1ccc(Br)c(N)n1
methyl 6-amino-5-bromopyridine-2-carboxylate
COC(=O)c1ccc2c(n1)NC(=O)CS2
ester
COC(=O)c1ccc2c(n1)NC(=O)CS2
Methyl 3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carboxylate

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cooled
  2. 2
    workup.ADDITION61, 1996, 4623-4633) was added
  3. 3
    洗涤washed with water (3×300 ml)
  4. 4
    其他dried
  5. 5
    其他evaporated to about 10 ml
  6. 6
    过滤The white solid was filtered off
  7. 7
    洗涤washed with a little EtOAc

实验过程

A solution of ethyl 2-mercaptoacetate (1.473 ml) in DMF (48 ml) was ice-cooled and treated with sodium hydride (540 mg of a 60% dispersion in oil). After 1 hour methyl 6-amino-5-bromopyridine-2-carboxylate (3 g) (T. R. Kelly and F. Lang, J. Org. Chem. 61, 1996, 4623-4633) was added and the mixture stirred for 16 hours at room temperature. The solution was diluted with EtOAc (1 litre), washed with water (3×300 ml), dried and evaporated to about 10 ml. The white solid was filtered off and washed with a little EtOAc to give the ester (0.95 g).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07498326B2uspto-grants-2009_03