反応 #53781

ord-ce84348b194c46e0a37af5ef56f97c3e

反応方程式

CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
Sodium triacetoxyborohydride
COC(=O)c1ccc(C=O)cc1
Methyl 4-formylbenzoate
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1N
5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine
O=C([O-])O.[Na+]
sodium bicarbonate
CC(=O)O
acetic acid
COC(=O)c1ccc(CNc2cc(-c3cc4cc(F)c(F)cc4[nH]3)ccc2OC)cc1
product
収率 26.7%
COC(=O)c1ccc(CNc2cc(-c3cc4cc(F)c(F)cc4[nH]3)ccc2OC)cc1
4-{[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenylamino]-methyl}-benzoic acid methyl ester
収率 26.7%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe resulting homogeneous solution stirred at room temperature for 4 days
  2. 2
    workup.STIRRINGthe mixture stirred for 2 hours
  3. 3
    workup.STIRRINGThe mixture was shaken
  4. 4
    その他the organic layer separated
  5. 5
    乾燥dried over Na2SO4
  6. 6
    その他The solvent was evaporated
  7. 7
    その他to give a brown gum
  8. 8
    その他Recrystallization from methanol

実験手順

Methyl 4-formylbenzoate (0.21 g, 1.28 mmol) was added to a stirred mixture of 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine (0.34 g, 1.24 mmol) in methylene chloride (125 mL), followed by acetic acid (0.3 g, 3.33 mmol). The resulting mixture was stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.3 g, 1.42 mmol) was added in one portion, and the resulting homogeneous solution stirred at room temperature for 4 days. Saturated aqueous sodium bicarbonate solution (100 mL) was added and the mixture stirred for 2 hours. The mixture was shaken, the organic layer separated, and dried over Na2SO4. The solvent was evaporated to give a brown gum. Recrystallization from methanol gave the product as off-white crystals (140 mg), mp 168-170° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06858739B2uspto-grants-2005_02