반응 #1747870

ord-503147315ea649f08e5d68cb04c58034

반응 방정식

c1ccc(-n2c(-c3ccc(N4c5ccccc5Sc5ccccc54)cc3)nc3ccccc32)cc1
10-[4-(N-phenyl-2-benzimidazolyl)phenyl]phenothiazine
O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
[K+].[OH-]
KOH
O=S1(=O)c2ccccc2N(c2ccc(-c3nc4ccccc4n3-c3ccccc3)cc2)c2ccccc21
10-[4-(N-Phenyl-2-benzimidazolyl)phenyl]phenothiazine 5,5-dioxide

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도with cooling
  2. 2
    기타After the methylene chloride had been removed
  3. 3
    workup.ADDITIONthe suspension was diluted with 100 ml of hot water
  4. 4
    여과The precipitate was filtered off with suction
  5. 5
    세척washed with hot water
  6. 6
    기타dried at 80° C. under reduced pressure
  7. 7
    기타The crude product (4.82 g) was recrystallized from 48 ml of acetic acid
  8. 8
    기타were obtained

실험 절차

A solution of 6.14 g of 10-[4-(N-phenyl-2-benzimidazolyl)phenyl]phenothiazine in 180 ml of methylene chloride was admixed at room temperature with 7.17 g (28.9 mmol) of 70% m-chloroperbenzoic acid with cooling and stirred at room temperature for 1 h. The solution was admixed with 60 ml of 10% KOH. After the methylene chloride had been removed, the suspension was diluted with 100 ml of hot water. The precipitate was filtered off with suction, washed with hot water and dried at 80° C. under reduced pressure. The crude product (4.82 g) was recrystallized from 48 ml of acetic acid. 3.02 g (46% of theory) of beige microcrystals having an m.p. of 286-288° C. were obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08029919B2uspto-grants-2011_10