تفاعل #53806

ord-e5680f1e35684a7e8e714f326cfd5c99

معادلة التفاعل

O=C([O-])O.[Na+]
sodium bicarbonate
O=Cc1ccc([N+](=O)[O-])cc1
4-Nitrobenzaldehyde
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1N
5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
Sodium triacetoxyborohydride
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc([N+](=O)[O-])cc1
product
المردود 55.0%
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc([N+](=O)[O-])cc1
[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-(4nitro-benzyl)-amine
المردود 55.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe resulting homogeneous solution was stirred at room temperature for 6 days
  2. 2
    workup.STIRRINGthe mixture was stirred for 2 hours
  3. 3
    workup.STIRRINGThe mixture was shaken
  4. 4
    أخرىthe organic layer was separated
  5. 5
    تجفيفdried over Na2SO4
  6. 6
    أخرىThe solvent was evaporated
  7. 7
    أخرىto give a red solid
  8. 8
    أخرىRecrystallization from methanol

الإجراء التجريبي

4-Nitrobenzaldehyde (0.3 g, 2.0 mmol) was added to a stirred mixture of 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine (0.548 g, 2.0 mmol) in methylene chloride (125 mL), followed by acetic acid (0.2 g). The resulting mixture was stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.46 g, 2.2 mmol) was added in one portion, and the resulting homogeneous solution was stirred at room temperature for 6 days. Saturated aqueous sodium bicarbonate solution (100 mL) was added, and the mixture was stirred for 2 hours. The mixture was shaken; the organic layer was separated and dried over Na2SO4. The solvent was evaporated to give a red solid. Recrystallization from methanol gave the product (450 mg), mp 181-182° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06858739B2uspto-grants-2005_02