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Hydrochloric Acid → Methyl 4-(1-benzyl-5-hexanamidoindol-3-ylmethyl)-3methoxybenzoate

HRID 275124
ノート
印刷プレビュー

反応式

HRID 275124 の反応式
CC(C)([O-])C.[K+].[C:7]([NH:14][C:15]1[CH:16]=[C:17]2[C:21](=[CH:22][CH:23]=1)[NH:20][CH:19]=[C:18]2[CH2:24][C:25]1[CH:34]=[CH:33][C:28]([C:29]([O:31][CH3:32])=[O:30])=[CH:27][C:26]=1[O:35][CH3:36])(=[O:13])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH2:37](Br)[C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1.Cl>O1CCCC1>[CH2:37]([N:20]1[C:21]2[C:17](=[CH:16][C:15]([NH:14][C:7](=[O:13])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])=[CH:23][CH:22]=2)[C:18]([CH2:24][C:25]2[CH:34]=[CH:33][C:28]([C:29]([O:31][CH3:32])=[O:30])=[CH:27][C:26]=2[O:35][CH3:36])=[CH:19]1)[C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=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 313Hydrochloric AcidHCID 7498Benzyl BromideHCID 23365832Methyl 4-(5-hexanamidoindol-3-ylmethyl)-3-methoxybenzoateHCID 23665647Potassium tert-butoxide

生成物 1

HCID 57133624Methyl 4-(1-benzyl-5-hexanamidoindol-3-ylmethyl)-3methoxybenzoate収率 22.1%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

Potassium t-butoxide (0.04 g.) was added to a stirred solution of methyl 4-(5-hexanamidoindol-3- ylmethyl)-3-methoxybenzoate (0.15 g.) in dry tetrahydrofuran (5 ml.), under an atmosphere of nitrogen. The resulting dark-green mixture was stirred for 30 minutes. Benzyl bromide (0.062 g.) was added, causing the color to change to light brown. After 1 hour, the mixture was poured into 1M hydrochloric acid (20 ml.). This mixture was extracted with ethyl acetate (2×25 ml.). The combined extracts were dried (MgSO4) and evaporated. The brown oil obtained was purified by flash chromatography on silica gel (50 ml.), eluting with 3:7 v/v ethyl acetate:hexane, to give the title compound (0.04 g, 17%) as an oil; NMR: 0.86 (t,3H, CH2.CH3) 1.27(m,4H, CH2.CH2.CH3), 1.57(m, 2H), CH2.CH2.CON), 2.24(t,2H, CH2.CH2. CON), 3.82(s,3H, CO.OCH3), 3.91(s,3H, OCH3), 3.99(s,2H, CH2.Ar), 5.32 (s,2H, NCH2Ph), 7.21(m,1OH), 7.44(m,2H), 7.75(d, 1H), 9.64(s,1H, NH).

後処理

  1. waitAfter 1 hour
  2. extractionThis mixture was extracted with ethyl acetate (2×25 ml.)
  3. dry with materialThe combined extracts were dried (MgSO4)
  4. customevaporated
  5. customThe brown oil obtained
  6. customwas purified by flash chromatography on silica gel (50 ml.)
  7. washeluting with 3:7 v/v ethyl acetate

出典と根拠

ORDレコード
ord-c79a9bb6a66d406a8f3f8842453a5a5d
出典データセット
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05391758

反応ノート

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