تفاعل #1135832

ord-d1975560a89a431db3aec296693becaf

معادلة التفاعل

[K+].[OH-]
KOH
COC(=O)CCCCCCc1nc2cc(Br)ccc2[nH]1
methyl 7-(5-bromo-1H-benzimidazol-2-yl)heptanoate
NO
hydroxylamine
O=C(CCCCCCc1nc2ccc(Br)cc2[nH]1)NO
7-(6-bromo-1H-benzimidazol-2-yl)-N-hydroxy heptanamide
المردود 52.8%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزbriefly concentrated
  2. 2
    workup.ADDITIONby adding 1 N HCl solution until pH was 7
  3. 3
    ترشيحThe light yellow precipitate was collected by filtration
  4. 4
    أخرىpump-dried

الإجراء التجريبي

To a solution of methyl 7-(5-bromo-1H-benzimidazol-2-yl)heptanoate (100 mg, 0.295 mmol) in THF at 0° C. was added 50% hydroxylamine solution (0.17 mL, 2.70 mmol). To this was added KOH (0.74 mL, 1M in MeOH, 0.74 mmol) dropwise. The reaction was stirred at 0° C. for 2 hr, briefly concentrated and neutralized by adding 1 N HCl solution until pH was 7. The light yellow precipitate was collected by filtration and pump-dried to give 7-(6-bromo-1H-benzimidazol-2-yl)-N-hydroxy heptanamide 15 (53 mg). The filtrate was extracted with ethyl acetate, dried and concentrated. The residue was purified by column to give another portion of the desired product 15 (16 mg). LCMS (M+1 @retention time): 340@1.283 min (LC conditions: 1. Column: YMC, C-18 ODS, 50×4.6 mm 0.5 u; 2. Mobile phase: A 0.05% TFA in water and B 0.05% TFA in acetonitrile; 3. Flow rate 1.2 mL/min; Gradient program: 20% B to 100% B in 3 min).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09381196B2uspto-grants-2016_07