تفاعل #969896

ord-c53fa5005666456c9f8f811cab450f7c

معادلة التفاعل

OB(O)c1ccccc1
phenyl boronic acid
O=P([O-])([O-])[O-].[K+].[K+].[K+]
potassium phosphate
CC1(C)C(=O)N(C2C3CC4CC(C3)CC2C4)C1C1(c2ccc(Br)cc2)CC1
1,4-dioxane
CC1(C)C(=O)N(C2C3CC4CC(C3)CC2C4)C1C1(c2ccc(Br)cc2)CC1
4-[1-(4-bromophenyl)cyclopropyl]-1-(adamantan-2-yl)-3,3-dimethylazetidin-2-one
CC1(C)C(=O)N(C2C3CC4CC(C3)CC2C4)C1C1(c2ccc(Br)cc2)CC1
4-[1-(4-bromophenyl)cyclopropyl]-1-(adamantan-2-yl)-3,3-dimethylazetidin-2-one
O
water
CC1(C)C(=O)N(C2C3CC4CC(C3)CC2C4)C1C1(c2ccc(-c3ccccc3)cc2)CC1
4-[1-(biphenyl-4-yl)cyclopropyl]-1-(adamantan-2-yl)-3,3-dimethylazetidin-2-one
المردود 84.0%

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate
  2. 2
    تجفيفThe organic layer was dried over anhydrous sodium sulfate
  3. 3
    تركيزconcentrated in vacuo
  4. 4
    أخرىThe obtained residue was purified

الإجراء التجريبي

A solution of 4-[1-(4-bromophenyl)cyclopropyl]-1-(adamantan-2-yl)-3,3-dimethylazetidin-2-one (12.2 mg, 0.0285 mmol) in 1,4-dioxane (3 mL) prepared in Example 75 was added with tetrakis(triphenylphosphine) palladium (1.6 mg, 1.4 μmol), phenyl boronic acid (7 mg, 0.057 mmol), and potassium phosphate (30 mg, 0.142 mmol) at room temperature, and the resultant was stirred at 100° C. for 20 hours. The reaction solution was poured into water, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo. The obtained residue was purified using thin-layer chromatography (hexane:ethyl acetate=3:1), and 4-[1-(biphenyl-4-yl)cyclopropyl]-1-(adamantan-2-yl)-3,3-dimethylazetidin-2-one (10.2 mg, 84%) was obtained as a white amorphous solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08236789B2uspto-grants-2012_08