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
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
- temperatureThen it was cooled again to −78° C.
- temperatureto warm to rt
- extractionextracted twice with ether
- extractionextracted several times with DCM
- washThe combined DCM extracts were then washed with brine
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- customthe solvent was evaporated
- customThe remaining residue was triturated with n-hexane
- 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
読み込み中…