反応 #338878

ord-f6c4fcb9254446ff855ad99595fc6fa1

反応方程式

O=C1Nc2ccc(F)cc2C1=Cc1cccc(C(=O)O)c1
3-((5-fluoro-2-oxoindolin-3-ylidene)methyl)benzoic acid
CCN=C=NCCCN(C)C.Cl
1-Ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride
Oc1cccc2[nH]nnc12
hydroxybenzo-triazole
CCN(CC)CC
triethylamine
COC(=O)CCCCCN.Cl
6-aminocaproic acid methyl ester hydrochloride
COC(=O)CCCCCNC(=O)c1cccc(C=C2C(=O)Nc3ccc(F)cc32)c1
title compound
収率 81.0%
COC(=O)CCCCCNC(=O)c1cccc(C=C2C(=O)Nc3ccc(F)cc32)c1
6-(3-((5-fluoro-2-oxoindolin-3-ylidene)methyl)benzamido)-hexanoic acid methyl ester
収率 81.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwere added
  2. 2
    ろ過The solids were collected by vacuum filtration
  3. 3
    洗浄washed with water
  4. 4
    その他dried under vacuum

実験手順

3-((5-fluoro-2-oxoindolin-3-ylidene)methyl)benzoic acid (283 mg, 1 mmol) and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (394 mg, 2 mmol), hydroxybenzo-triazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and 6-aminocaproic acid methyl ester hydrochloride (219 mg, 1.2 mmol) were added. The mixture was stirred for 24 hours at room temperature. The mixture was diluted with 400 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (332 mg, 81% yield) as a brown solid. LC-MS (m/z) 411 (M+1).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07863315B2uspto-grants-2011_01