Carbon Dioxide → 5-methyl-1H-indole-7-carboxylic acid

HRID 855280

反応式

HRID 855280 の反応式
Br[C:2]1[CH:3]=[C:4]([CH3:11])[CH:5]=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2.[Li]CCCC.[C:17](=[O:19])=[O:18].O>C1COCC1.CCCCCC>[CH3:11][C:4]1[CH:5]=[C:6]2[C:10](=[C:2]([C:17]([OH:19])=[O:18])[CH:3]=1)[NH:9][CH:8]=[CH:7]2

参加物

7

反応条件

温度
2.5 °C

実験手順

1.68 g of 7-bromo-5-methyl-indole (8 mmol) were dissolved in 30 ml THF and 15 ml of a 1.6 molar solution of n-BuLi in hexane were added at −78° C. The reaction mixture was then allowed to warm to 0-5° C. and was stirred at this temperature for 30 min. Then it was cooled again to −78° C., dry ice was added and the mixture was allowed to warm to rt. After 15 min at rt it was poured into water and extracted twice with ether. The aqueous phase was then acidified with 1 N HCl solution and extracted several times with DCM. The combined DCM extracts were then washed with brine, dried with magnesium sulfate, filtered and the solvent was evaporated. The remaining residue was triturated with n-hexane. Final filtration yielded 0.78 g (56%) of 5-methyl-1H-indole-7-carboxylic acid as light brown solid. 1H NMR (DMSO-d, 300 MHz): δ 2.41 (s, 3H), 6.44 (m, 1H), 7.31 (m, 1H), 7.58 (s, 1H), 7.61 (s, 1H), 10.91 (br s, 1H), 12.92 (br s, 1H).

後処理

  1. temperatureThen it was cooled again to −78° C.
  2. temperatureto warm to rt
  3. extractionextracted twice with ether
  4. extractionextracted several times with DCM
  5. washThe combined DCM extracts were then washed with brine
  6. dry with materialdried with magnesium sulfate
  7. filtrationfiltered
  8. customthe solvent was evaporated
  9. customThe remaining residue was triturated with n-hexane
  10. filtrationFinal filtration

出典と根拠

ORDレコード
ord-5721f061e67e4ef3ada7bb121c21c9a0
出典データセット
uspto-grants-2007_08
特許番号
US07259183B2

関連ノート

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