反应 #2122513

ord-097b5858728d43679c2f44d922bf93e1

反应方程式

Cc1nc2ccc(S(=O)(=O)Cl)cc2s1
Compound 2
Cc1nc2ccc(S(=O)(=O)Cl)cc2s1
2-methylbenzothiazole-6-sulfonyl chloride
C1CCNCC1
piperidine
CCCCCC
hexane
Cc1nc2ccc(S(=O)(=O)N3CCCCC3)cc2s1
Compound 3
收率 74.2%
Cc1nc2ccc(S(=O)(=O)N3CCCCC3)cc2s1
N-(2-methylbenzothiazole-6-sulfonyl)piperidine
收率 74.2%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤The reaction mixture was then washed with water (2×, 50 ml) and brine (1×, 50 ml)
  2. 2
    干燥The organic layer was dried with sodium sulfate
  3. 3
    其他evaporated
  4. 4
    其他The sticky white solid thus obtained
  5. 5
    其他The white solid that precipitated
  6. 6
    其他was collected
  7. 7
    洗涤washed with hexane
  8. 8
    其他dried

实验过程

A solution of Compound 2 (2.5 g, 10 mmol) in chloroform (15 ml) was added drop wise to a solution of piperidine (1.7 g, 20.0 mmol) in chloroform (10 ml). The combined mixture was stirred at room temperature for 1 hour. The reaction mixture was then washed with water (2×, 50 ml) and brine (1×, 50 ml). The organic layer was dried with sodium sulfate and evaporated. The sticky white solid thus obtained was dissolved in ca. 5 ml of hot ethyl acetate and this solution was then slowly added to 40 ml hexane. The white solid that precipitated was collected, washed with hexane and dried to yield 2.2 g (74%) of Compound 3, Rf=0.28 (30% ethyl acetate in hexane). The structure of Compound 3 is given below:

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08574881B2uspto-grants-2013_11