تفاعل #1144429

ord-907b2baf85be45e89b06298c744d836e

معادلة التفاعل

Cc1c(-c2ccccc2)[nH]c(=S)[nH]c1=O
6-phenythiothymine
Cc1ccc(S(=O)(=O)[O-])cc1CCCCO[Si](C)(C)C(C)(C)C
4-(t-butyldimethylsiloxy)-butyl-p-toluenesulphonate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1c(-c2ccccc2)n(CCCCO)c(=S)[nH]c1=O
target compound
المردود 4.1%
Cc1c(-c2ccccc2)n(CCCCO)c(=S)[nH]c1=O
1-(4-hydroxybutyl) -6-phenylthiothymine
المردود 4.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةheated
  2. 2
    أخرىto react for 4 hours at 80° C
  3. 3
    تركيزThe reaction mixture was concentrated under reduced pressure
  4. 4
    workup.ADDITIONadded with methanol
  5. 5
    ترشيحfiltered
  6. 6
    تركيزThe filtrate was concentrated under reduced pressure
  7. 7
    workup.ADDITIONadded with 20 ml of tetrahydrofuran and 1 ml of 1N hydrochloric acid
  8. 8
    تركيزThe reaction mixture was concentrated under reduced pressure
  9. 9
    غسيلeluted with 2% methanol/chloroform The eluate
  10. 10
    تركيزwas concentrated
  11. 11
    أخرىcrystallized from acetone/hexane

الإجراء التجريبي

To 2 ml of dimethyl sulfoxide, 468 mg (2.0 mmol) of 6-phenythiothymine, 358 mg (1.0 mmol) of 4-(t-butyldimethylsiloxy)-butyl-p-toluenesulphonate and 276 mg (2.0 mmol) of potassium carbonate were added and heated to react for 4 hours at 80° C. The reaction mixture was concentrated under reduced pressure, added with methanol and filtered. The filtrate was concentrated under reduced pressure, added with 20 ml of tetrahydrofuran and 1 ml of 1N hydrochloric acid and stirred for 90 minutes. The reaction mixture was concentrated under reduced pressure and adsorbed on a silica gel column and eluted with 2% methanol/chloroform The eluate was concentrated and crystallized from acetone/hexane to obtain 12.0 mg of the target compound (Yield: 4%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE037979E1uspto-grants-2003_02