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Sodium hydride → 1-[3-{2(E)-(7-Chloroquinolin-2-yl)ethenyl}benzyl]-7-trityloxy-indole

HRID 1198537
ノート
印刷プレビュー

反応式

HRID 1198537 の反応式
[H-].[Na+].[C:3]([O:22][C:23]1[CH:24]=[CH:25][CH:26]=[C:27]2[C:31]=1[NH:30][CH:29]=[CH:28]2)([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Cl:32][C:33]1[CH:42]=[C:41]2[C:36]([CH:37]=[CH:38][C:39](/[CH:43]=[CH:44]/[C:45]3[CH:46]=[C:47]([CH:50]=[CH:51][CH:52]=3)[CH2:48]Cl)=[N:40]2)=[CH:35][CH:34]=1.[Cl-].[NH4+]>CN(C)C=O>[Cl:32][C:33]1[CH:42]=[C:41]2[C:36]([CH:37]=[CH:38][C:39](/[CH:43]=[CH:44]/[C:45]3[CH:46]=[C:47]([CH:50]=[CH:51][CH:52]=3)[CH2:48][N:30]3[C:31]4[C:27](=[CH:26][CH:25]=[CH:24][C:23]=4[O:22][C:3]([C:16]4[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=4)([C:10]4[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=4)[C:4]4[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=4)[CH:28]=[CH:29]3)=[N:40]2)=[CH:35][CH:34]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 150540107-(Triphenylmethoxy)-1H-indoleHCID 19369489trans-3-[2-(7-Chloroquinolin-2-yl)ethenyl]benzyl chloride

生成物 1

HCID 191026091-[3-{2(E)-(7-Chloroquinolin-2-yl)ethenyl}benzyl]-7-trityloxy-indole

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒
2 回

実験手順

60% Sodium hydride dispersion in mineral oil (44 mg 1.1 mmol) was added to a stirred solution of 7-trityloxyindole (Example 12a) (375 mg, 1.0 mmol) in dimethylformamide (4 ml). The mixture was stirred for 10 minutes at room temperature then a suspension of 3-[2(E)-(7-chloroquinolin-2-yl)ethenyl]benzyl chloride (Example 6a) (251 mg, 0.80 mmol) in dimethylformamide (4 ml) was added and the mixture was stirred for a further 3 hours. The dark solution was poured onto saturated ammonium chloride solution and extracted with dichloromethane. The extract was dried and evaporated under high vacuum and the residue was chromatographed on silica in ethyl acetate-hexane (1:5).

後処理

  1. additionwas added
  2. stirringthe mixture was stirred for a further 3 hours
  3. extractionextracted with dichloromethane
  4. customThe extract was dried
  5. customevaporated under high vacuum
  6. customthe residue was chromatographed on silica in ethyl acetate-hexane (1:5)

出典と根拠

ORDレコード
ord-527e08840fc54af29c1c52875be36008
出典データセット
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05281593

反応ノート

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