Water → n-Methyl-1-(1-methyl-1h-indol-5-yl)methanamine

HRID 1711828

反応式

HRID 1711828 の反応式
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([CH:11]=O)=[CH:8][CH:9]=2)[CH:4]=[CH:3]1.[CH3:13][NH2:14].[BH4-].[Na+].O>CO>[CH3:13][NH:14][CH2:11][C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[N:2]([CH3:1])[CH:3]=[CH:4]2

参加物

6

実験手順

N-Methylindole-5-carbaldehyde (800 mg, 5.1 mmol) was dissolved in anhydrous methanol (15 mL). Methylamine (7.15 mL of 2M solution in methanol, 15.3 mmol) was added and the reaction was stirred for 3 hr. The solution was concentrated to a yellow oil and then dissolved into anhydrous methanol (15 mL). Sodium borohydride (194 mg, 5.1 mmol) was added and the mixture was stirred overnight. Water (1 mL) was added and the solution was concentrated to an orange oil. Sodium hydroxide (5 mL, 1N) was added and the product was extracted with ethyl acetate (3×20 mL), dried over MgSO4 and concentrated to afford the title compound as an orange oil (885 mg, 100%). 1H NMR (200 MHz, CDCl3) δ 7.57(s, 1H), 7.35-7.11(m, 3H), 6.51 (d, J=2.9 Hz, 1H), 3.85 (s, 2H), 3.79 (s, 3H), 2.48 (s, 3H).

後処理

  1. concentrationThe solution was concentrated to a yellow oil
  2. dissolutiondissolved into anhydrous methanol (15 mL)
  3. stirringthe mixture was stirred overnight
  4. concentrationthe solution was concentrated to an orange oil
  5. additionSodium hydroxide (5 mL, 1N) was added
  6. extractionthe product was extracted with ethyl acetate (3×20 mL)
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-21504158dc084497ad3ae3acd4fdeae6
出典データセット
uspto-grants-2010_09
特許番号
US07790709B2

関連ノート

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