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Diethyl Ether → HCID 59277534、化合物

HRID 1362451
ノート
印刷プレビュー

反応式

HRID 1362451 の反応式
C([Li])(C)(C)C.CC[O:8][CH2:9][CH3:10].Br[C:12]1[CH:13]=[C:14]2[C:18](=[CH:19][C:20]=1C)[NH:17][CH:16]=[C:15]2[CH3:22]>CN(C=O)C>[CH3:22][C:15]1[C:14]2[C:18](=[CH:19][C:20]([CH3:12])=[C:10]([CH:9]=[O:8])[CH:13]=2)[NH:17][CH:16]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3283Diethyl EtherHCID 59277605HCID 59277605、化合物HCID 178418306HCID 178418306、化合物

生成物 1

HCID 59277534HCID 59277534、化合物収率 82%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

tert-Butyl lithium (16.7 mL, 28.3 mmol, 1.7 M in pentanes) was added to a dry ether (20 mL) solution of 5-bromo-3,6-dimethyl-1H-indole (1.27 g, 5.67 mmol) at −78° C. under Argon. The mixture was stirred at 0° C. for 30 min then cooled to −78° C. DMF (18 mL) was added and the mixture was stirred at 0° C. for 1 h. The reaction was quenched with cold, saturated NH4Cl solution at −78° C. The mixture was diluted with ether and hexane, washed with brine, dried and evaporated. Crystallization from a CH2Cl2/hexane mixture afforded the title compound (810 mg 82%). 1H NMR (300 MHz, CDCl3) 10.29 (s, 1H), 8.06 (s, 1H), 8.00 (s, br, 1H), 7.15 (1s, 1H), 6.97 (s, 1H), 2.76 (s, 3H), 2.36 (s, 3H).

後処理

  1. temperaturethen cooled to −78° C
  2. stirringthe mixture was stirred at 0° C. for 1 h
  3. customThe reaction was quenched with cold, saturated NH4Cl solution at −78° C
  4. additionThe mixture was diluted with ether and hexane
  5. washwashed with brine
  6. customdried
  7. customevaporated
  8. customCrystallization from a CH2Cl2/hexane mixture

出典と根拠

ORDレコード
ord-9c56efd0035a404bb95e74c2fb22a2be
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07879872B2

反応ノート

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