تفاعل #1836349

ord-9fdc3a9112ee4896a2ca4f2715741251

معادلة التفاعل

COc1cccc(NCC(O)Cn2c3ccc(Br)cc3c3cc(Br)ccc32)c1
1-(3,6-dibromo-9H-carbazol-9-yl)-3-(3-methoxyphenylamino)propan-2-ol
CCN(CC)CC
triethylamine
COc1cccc(NCC(=O)Cn2c3ccc(Br)cc3c3cc(Br)ccc32)c1
1-(3,6-dibromo-9H-carbazol-9-yl)-3-(3-methoxyphenylamino)-propan-2-one

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGAfter stirring overnight
  2. 2
    أخرىfollowed by sulfur trioxide pyridine complex (0.663 mg, 4.17 mmol) an hour
  3. 3
    workup.STIRRINGAfter stirring for 1 h
  4. 4
    غسيلwashed several times with water

الإجراء التجريبي

Trietheylamine (1.65 ml, 11.8 mmol) was added to a stirring solution of 1-(3,6-dibromo-9H-carbazol-9-yl)-3-(3-methoxyphenylamino)propan-2-ol (1.02 g, 2.02 mmol) in DMSO (21 ml). The solution was stirred for 30 minutes before addition of sulfur trioxide pyridine complex (0.659 g, 4.14 mmol). After stirring overnight, additional triethylamine (1.0 ml, 7.17 mmol) was added, followed by sulfur trioxide pyridine complex (0.663 mg, 4.17 mmol) an hour later. After stirring for 1 h, the orange solution was diluted with ˜150 ml ethyl acetate and washed several times with water and then brine.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09156787B2uspto-grants-2015_10