反应 #1726701

ord-300f7a02978d426eb436c3b0049ef3dc

反应方程式

N
ammonia
NN
hydrazine
O=S(=O)(Cl)Cl
sulfonyl chloride
O=C1c2ccccc2C(=O)N1c1scnc1-c1ccccc1
4-phenyl-5-phthalimido-thiazole
NN
hydrazine
Nc1sc(S(N)(=O)=O)nc1-c1ccccc1
5-amino-2-(aminosulfonyl)-4-phenylthiazole
收率 36.0%
Nc1scnc1-c1ccccc1
5-amino-4-phenylthiazole
收率 16.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩After 10 min the mixture was concentrated in vacuo
  2. 2
    温度heated to reflux
  3. 3
    温度reflux
  4. 4
    过滤The cooled mixture was filtered
  5. 5
    浓缩concentrated in vacuo

实验过程

The crude mixture of sulfonyl chloride with 4-phenyl-5-phthalimido-thiazole (231 mg) in dichloromethane (10 ml) was treated with ammonia in methanol (900 μl, 2.0 M) dropwise at ambient temperature. After 10 min the mixture was concentrated in vacuo. The residue was suspended in ethanol (10 ml), treated with ethanolic hydrazine (660 μl, 1.0 M, 660 μmol) and heated to reflux. After 1.5 hr a further portion of ethanolic hydrazine was added (660 μl, 1.0 M, 660 mol) and reflux continued for 15 hr. The cooled mixture was filtered and concentrated in vacuo. Flash chromatography on silica gel (ethyl acetate/hexanes) yielded pure 5-amino-2-(aminosulfonyl)-4-phenylthiazole (56 mg, 36% for 3 steps) and 5-amino-4-phenylthiazole (17 mg, 16% for 3 steps).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08110568B2uspto-grants-2012_02