تفاعل #595391

ord-f323e5b16b5249e3bfc4a7d5a49e5ca0

معادلة التفاعل

COc1cccc(N(CC(F)Cn2c3ccc(Br)cc3c3cc(Br)ccc32)S(=O)(=O)c2ccc([N+](=O)[O-])cc2)c1
N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-N-(3-methoxyphenyl)-4-nitrobenzenesulfonamide
[Li+].[OH-]
lithium hydroxide
CN(C)C=O
dimethylformamide
O=C(O)CS
mercaptoacetic acid
COc1cccc(NCC(F)Cn2c3ccc(Br)cc3c3cc(Br)ccc32)c1
N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-3-methoxyaniline
المردود 88.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed sequentially with water, saturated sodium bicarbonate solution, water (3×) and brine
  2. 2
    تجفيفThe organic layer was dried over Na2SO4
  3. 3
    ترشيحfiltered
  4. 4
    أخرىcondensed
  5. 5
    أخرىThe crude reaction mixture
  6. 6
    أخرىwas purified in 30% EtOAc/hexanes (+0.2% TEA), with 13.6 mg
  7. 7
    أخرىisolated

الإجراء التجريبي

To a vial containing N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-N-(3-methoxyphenyl)-4-nitrobenzenesulfonamide (21.0 mg, 0.030 mmol; see representative procedure 4) was added lithium hydroxide (3.2 mg, 0.134 mmol), dimethylformamide (0.5 ml, 0.06 M) and mercaptoacetic acid (4.2 ul 0.060 mmol). After stirring at rt for 1 h the reaction mixture was diluted with EtOAc and washed sequentially with water, saturated sodium bicarbonate solution, water (3×) and brine. The organic layer was dried over Na2SO4, filtered and condensed. The crude reaction mixture was purified in 30% EtOAc/hexanes (+0.2% TEA), with 13.6 mg isolated. Yield=88%

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09095572B2uspto-grants-2015_08