تفاعل #340193

ord-c791e66a12fc4a3aa48fc8ccb15ad938

معادلة التفاعل

Cl
hydrochloric acid
O=C([O-])[O-].[K+].[K+]
Potassium carbonate
O=[N+]([O-])c1ccccc1S(=O)(=O)Oc1ccc(C2CN(S(=O)(=O)c3ccccc3[N+](=O)[O-])CCO2)cc1
title compound
O=[N+]([O-])c1ccccc1S(=O)(=O)Oc1ccc(C2CN(S(=O)(=O)c3ccccc3[N+](=O)[O-])CCO2)cc1
4-(4-(2-Nitrobenzenesulfonyl)morpholin-2-yl)phenyl 2-nitrobenzenesulfonate
Sc1ccc(Br)cc1
4-bromobenzenethiol
Oc1ccc(C2CNCCO2)cc1
title compound
المردود 63.5%
Oc1ccc(C2CNCCO2)cc1
4-(Morpholin-2-yl)phenol
المردود 63.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred at room temperature for 3.5 hr
  2. 2
    غسيلThe aqueous layer was washed with ethyl acetate
  3. 3
    تركيزwas concentrated to dryness under the reduced pressure
  4. 4
    workup.ADDITIONMethanol was added to the residue
  5. 5
    ترشيحthe mixture was filtered
  6. 6
    تركيزThe filtrate was concentrated under the reduced pressure
  7. 7
    أخرىthe residue was purified by column chromatography on silica gel (chloroform:methanol=20:1, chloroform:methanol:28% aqueous ammonia=9:2:0.2)

الإجراء التجريبي

Potassium carbonate (0.88 g, 6.33 mmol) was added to a solution of 1.16 g (2.11 mmol) of the title compound produced in step (iii) of Reference Example 12 in N,N-dimethylformamide (8.5 ml), and the mixture was stirred at room temperature for 5 min. Next, 1.20 g (6.33 mmol) of 4-bromobenzenethiol was added thereto, and the mixture was stirred at room temperature for 3.5 hr. The reaction was stopped by adding 1 N hydrochloric acid, and the reaction solution was adjusted to pH=3. The aqueous layer was washed with ethyl acetate and was concentrated to dryness under the reduced pressure. Methanol was added to the residue, and the mixture was filtered, The filtrate was concentrated under the reduced pressure, and the residue was purified by column chromatography on silica gel (chloroform:methanol=20:1, chloroform:methanol:28% aqueous ammonia=9:2:0.2) to give 240 mg (yield 63%) of the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07871982B2uspto-grants-2011_01