تفاعل #1269891

ord-46160462a979401a929b3686ce488800

معادلة التفاعل

[BH4-].[Na+]
NaBH4
CCCCN1Cc2cc(N)ccc2C1=O
5-Amino-2-butylisoindolin-1-one
CC(C)(C)C(=O)Nc1ccncc1C=O
N-(3-formylpyridin-4-yl)pivalamide
O=C([O-])O.[Na+]
NaHCO3
O=C([O-])O.[Na+]
NaHCO3
CCCCN1Cc2cc(NCc3cnccc3NC(=O)C(C)(C)C)ccc2C1=O
crude product
CCCCN1Cc2cc(NCc3cnccc3NC(=O)C(C)(C)C)ccc2C1=O
N-(3-((2-butyl-1-oxoisoindolin-5-ylamino)methyl)pyridin-4-yl)pivalamide

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added
  2. 2
    استخلاصThe mixture was extracted with EtOAc
  3. 3
    غسيلthe combined organic layers were washed with water
  4. 4
    تجفيفdried over MgSO4
  5. 5
    أخرىthe solvent was removed in vacuo
  6. 6
    أخرىThe residue obtained
  7. 7
    استخلاصExtraction with EtOAc
  8. 8
    غسيلwashing of the combined organic layers with water
  9. 9
    تجفيفdrying over MgSO4

الإجراء التجريبي

5-Amino-2-butylisoindolin-1-one (49.5 mg, 0.242 mmol) was added to a solution of N-(3-formylpyridin-4-yl)pivalamide (50 mg, 0.242 mmol) in acetic acid (1 mL). After stiffing for 5 days, water and sat aqueous NaHCO3 solution were added. The mixture was extracted with EtOAc, the combined organic layers were washed with water, dried over MgSO4 and the solvent was removed in vacuo. The residue obtained was dissolved in MeOH (3 mL) and NaBH4 (18.3 mg, 0.485 mmol) was added. After stirring overnight, water and sat. aqueous NaHCO3 solution were added. Extraction with EtOAc, washing of the combined organic layers with water and drying over MgSO4 provided the crude product which was purified by HPLC (24 mg, 19%). ESI-MS [M+H]+=395.2.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08664214B2uspto-grants-2014_03