تفاعل #45887

ord-81fd409dc70646578783faff6114b640

معادلة التفاعل

C=C(C)c1c(C)c(C#N)c2nc(C3CC3)oc2c1F
2-Cyclopropyl-7-fluoro-6-isopropenyl-5-methyl-1,3-benzoxazole-4-carbonitrile
CCN(CC)CC
triethylamine
CN(C)[C@H]1CCNC1
(3S)-3-(dimethylamino)pyrrolidine
C=C(C)c1c(C)c(C#N)c2nc(C3CC3)oc2c1N1CC[C@H](N(C)C)C1
compound
المردود 46.1%
C=C(C)c1c(C)c(C#N)c2nc(C3CC3)oc2c1N1CC[C@H](N(C)C)C1
2-Cyclopropyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-6-isopropenyl-5-methyl-1,3-benzoxazole-4-carbonitrile
المردود 46.1%

المذيبات

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAfter cooled
  2. 2
    تركيزthis was concentrated under reduced pressure
  3. 3
    workup.ADDITIONdiluted with chloroform
  4. 4
    غسيلwashed with saturated brine
  5. 5
    تجفيفThe organic layer was dried over anhydrous magnesium sulfate
  6. 6
    أخرىthe solvent was evaporated away under reduced pressure
  7. 7
    أخرىThe resulting residue was purified by preparative TLC (eluent, chloroform

الإجراء التجريبي

2-Cyclopropyl-7-fluoro-6-isopropenyl-5-methyl-1,3-benzoxazole-4-carbonitrile (I-315) (34 mg, 0.13 mmol) was dissolved in dimethyl sulfide (2 ml), then triethylamine (38 μl, 0.27 mmol) and (3S)-3-(dimethylamino)pyrrolidine (36 μl, 0.28 mmol) were added, followed by stirring under nitrogen atmosphere at 90° C. for 4 hours. After cooled, this was concentrated under reduced pressure, diluted with chloroform and washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate, then the solvent was evaporated away under reduced pressure. The resulting residue was purified by preparative TLC (eluent, chloroform:methanol=10:1, v/v) to obtain the entitled compound (21 mg, 25%) as a brown crystal.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07737166B2uspto-grants-2010_06