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Lithium hydroxide, monohydrate → 3-Methoxy-4-[1-methyl-5-[2-(pentylcarbamoyl)propyl]indol-3-ylmethyl]benzoic acid

HRID 330179
ノート
印刷プレビュー

反応式

HRID 330179 の反応式
O.[OH-].[Li+].[CH3:4][O:5][C:6]1[CH:7]=[C:8]([CH:13]=[CH:14][C:15]=1[CH2:16][C:17]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([CH2:26][CH:27]([C:29](=[O:36])[NH:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])[CH3:28])[CH:24]=2)[N:19]([CH3:37])[CH:18]=1)[C:9]([O:11]C)=[O:10]>O.CO.O1CCCC1>[CH3:4][O:5][C:6]1[CH:7]=[C:8]([CH:13]=[CH:14][C:15]=1[CH2:16][C:17]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([CH2:26][CH:27]([C:29](=[O:36])[NH:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])[CH3:28])[CH:24]=2)[N:19]([CH3:37])[CH:18]=1)[C:9]([OH:11])=[O:10]
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 2

HCID 168937Lithium hydroxide, monohydrateHCID 14882559Methyl 3-methoxy-4-[1-methyl-5-[2-(pentylcarbamoyl)propyl]indol-3-ylmethyl]benzoate

生成物 1

HCID 198706133-Methoxy-4-[1-methyl-5-[2-(pentylcarbamoyl)propyl]indol-3-ylmethyl]benzoic acid収率 99.9%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

A solution of lithium hydroxide monohydrate (0.29 g) in water (5 ml) was added to a solution of methyl 3-methoxy-4-[1-methyl-5-[2-(pentylcarbamoyl)propyl]indol-3-ylmethyl]benzoate (0.65 g) in methanol (25 ml) and tetrahydrofuran (5 ml). The mixture was stirred under an atmosphere of nitrogen for 48 hr, and the solvents evaporated. The residue was taken up in water (5 ml), acidified with 1M hydrochloric acid (10 ml), and the precipitate which formed isolated by filtration to give the title compound (0.63 g, 94%) as a white powder; mp 85°-95°.

後処理

  1. customthe solvents evaporated
  2. customthe precipitate which formed
  3. customisolated by filtration

出典と根拠

ORDレコード
ord-78e0068d84ab423bbedc0145bf8d41aa
出典データセット
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04894386

反応ノート

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