反応 #93243

ord-20c05777869649cbb7f50673712d87e4

反応方程式

O=C([O-])O.[Na+]
NaHCO3
Nc1ccccc1S
2-aminothiophenol
O=C1C=CC(=O)C2CC=CCC12
4a, 5, 8, 8a-tetrahydro-1,4-naphtoquinone
Cl
HCl
Oc1cc2c(c3c1CC=CC3)Nc1ccccc1S2
title compound
Oc1cc2c(c3c1CC=CC3)Nc1ccccc1S2
5-Hydroxy-1,4-dihydro-12H-benzo[a]phenothiazine

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe mixture was stirred for another 2 hours
  2. 2
    その他The organic layer was decanted
  3. 3
    その他dried
  4. 4
    その他evaporated to dryness
  5. 5
    その他The resulting oily residue was chromatographed on silica gel (CH2Cl2)

実験手順

A solution of 2-aminothiophenol (385 mg) in methanol (3 ml) was added to a solution of 4a, 5, 8, 8a-tetrahydro-1,4-naphtoquinone (Ref.: Ber. 62, 2361 (1929)) (500 mg) in methanol (10 ml) and stirred for 1 hour. Then conc. HCl (2 ml) was added and the mixture was stirred for another 2 hours. Ethyl acetate was added to the reaction mixture followed by a solution of NaHCO3. The organic layer was decanted, dried and evaporated to dryness. The resulting oily residue was chromatographed on silica gel (CH2Cl2) to afford the title compound.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04611056uspto-grants-1986_09