N,N'-Dimethylethylenediamine → 1-Isopropyl-3-methyl-6-(methylsulfonyl)-1H-indole-4-carboxylic acid

HRID 42515

反応式

HRID 42515 の反応式
Br[C:2]1[CH:3]=[C:4]([C:15]([O:17]C)=[O:16])[C:5]2[C:6]([CH3:14])=[CH:7][N:8]([CH:11]([CH3:13])[CH3:12])[C:9]=2[CH:10]=1.[CH3:19][S:20]([OH:22])=[O:21].CNCCNC>CS(C)=O>[CH:11]([N:8]1[C:9]2[CH:10]=[C:2]([S:20]([CH3:19])(=[O:22])=[O:21])[CH:3]=[C:4]([C:15]([OH:17])=[O:16])[C:5]=2[C:6]([CH3:14])=[CH:7]1)([CH3:13])[CH3:12]

参加物

5

反応条件

温度
165 °C

実験手順

To a 30-mL microwave tube were added methyl 6-bromo-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylate (490 mg, 1.580 mmol), methanesulfinic acid (212 mg, 2.054 mmol), DMSO (7 mL), N,N′-dimethyl-1,2-ethanediamine (18.10 mg, 0.205 mmol), and the mixture was degassed for 5 min by bubbling N2. Copper(I) trifluoromethanesulfonate benzene complex (63.6 mg, 0.126 mmol) was added and the tube was sealed. The mixture was heated at 165° C. overnight with stirring. The mixture was allowed to cool, filtered and purified using reverse-phase HPLC (Gemini 5u C18(2) 100A, AXIA; 30×100 mm 5 micron; 30 mL/min, 30% ACN/H2O, 0.1% formic acid to 60% ACN/H2O, 0.1% formic acid) to give the title compound (118 mg, 25%) as a white solid. 1H NMR (400 MHz, DMSO-d6) ppm 1.47 (d, J=8.00 Hz, 6H), 2.30-2.41 (m, 3H), 4.94 (quin, J=6.63 Hz, 1H), 7.80 (s, 1H), 7.88 (d, J=1.77 Hz, 1H), 8.24 (d, J=1.52 Hz, 1H), 13.17 (br. s., 1H). MS: (M+H)+296.3.

後処理

  1. customthe mixture was degassed for 5 min
  2. customby bubbling N2
  3. additionCopper(I) trifluoromethanesulfonate benzene complex (63.6 mg, 0.126 mmol) was added
  4. customthe tube was sealed
  5. temperatureto cool
  6. filtrationfiltered
  7. custompurified

出典と根拠

ORDレコード
ord-d9eb2c1de85f4693bc78e0c72d712ed1
出典データセット
uspto-grants-2013_09
特許番号
US08536179B2

関連ノート

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