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Methanol → 2-(2-Adamantyloxycarbonyl)amino-3-(3-indolyl)butanoic acid

HRID 1457243
ノート
印刷プレビュー

反応式

HRID 1457243 の反応式
[NH2:1][CH:2]([CH:6]([C:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[NH:10][CH:9]=1)[CH3:7])[C:3]([OH:5])=[O:4].C(=O)([O-])O.[Na+].Cl[C:23]([O:25][CH:26]1[CH:33]2[CH2:34][CH:29]3[CH2:30][CH:31]([CH2:35][CH:27]1[CH2:28]3)[CH2:32]2)=[O:24].CO>[OH-].[Na+].O1CCOCC1.ClCCl>[CH:33]12[CH2:34][CH:29]3[CH2:30][CH:31]([CH2:35][CH:27]([CH2:28]3)[CH:26]1[O:25][C:23]([NH:1][CH:2]([CH:6]([C:8]1[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[NH:10][CH:9]=1)[CH3:7])[C:3]([OH:5])=[O:4])=[O:24])[CH2:32]2
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 887MethanolHCID 2921702-Amino-3-(3-indolyl)butanoic acidHCID 516892Sodium BicarbonateHCID 108785372-adamantyl Chloroformate

生成物 1

HCID 221022962-(2-Adamantyloxycarbonyl)amino-3-(3-indolyl)butanoic acid収率 63%

試薬・触媒・溶媒 3

HCID 6344
Dichloromethane
溶媒
HCID 14798Sodium Hydroxide溶媒
HCID 312751,4-Dioxane溶媒2 回

実験手順

Percent amino acid (75) (449 mg, 2.29 mmol) in 1N sodium hydroxide (2.29 mL) was added to sodium hydrogen carbonate (211 mg, 2.5 mmol). This mixture was cooled to 0° C. (ice bath), dioxan. (2.29 mL) was added, followed by dropwise addition with stirring of a solution of the chloroformate (76) (742 mg, 34.46 mmol) in dioxan (2.29 mL). When all the amino acid had gone (TLC SiO2 :4% methanol in dichloromethane), the dioxan was removed in vacuo and the residue partitioned between 10% citric acid and ethyl acetate. The aqueous phase was extracted further with ethyl acetate. The organic extracts were combined, dried (MgSO4), and evaporated to dryness. The crude acid was purified by column chromatography on normal silica [hexane:ethyl acetate (3:20+0.5% acetic acid as eluant] to give 2-(2-adamantyloxy-carbonyl)amino-3-(3-indolyl) butanoic acid (77) (570 mg, 63%); δ H (300 M Hz, d6 -DMSO), 1.34 (3H, d, J 8Jz. CH3), 1.68-2.00 (14H, m, adamantyl), 3.40-3.53 (1H, m, indCH(CH3)), 4.36 (1H, brt, CH(CO2H)), 4.59 (1H, s, adamantyl 2-H), 6.73 (1H, d, J 9 Hz, urethane NH), 6.96 (1H, t, J 7 Hz, indole 5-H), 7.06m (1H, t, J 7 Hz, indole 6-H), 7.17 (1H, brs, indole 2-H), 7.33 (1H, d, J 8 Hz, indole 7-H), 7.60 (1H, d, J 8 Hz, indole 4-H), 10.83 (1H, s, indole NH)m, ca 12.6 (vbrs, CO2H).

後処理

  1. addition(2.29 mL) was added
  2. additionfollowed by dropwise addition
  3. customthe dioxan was removed in vacuo
  4. customthe residue partitioned between 10% citric acid and ethyl acetate
  5. extractionThe aqueous phase was extracted further with ethyl acetate
  6. dry with materialdried (MgSO4)
  7. customevaporated to dryness
  8. customThe crude acid was purified by column chromatography on normal silica [hexane:ethyl acetate (3:20+0.5% acetic acid as eluant]

出典と根拠

ORDレコード
ord-c6c064e126c84fef86ae13897c36f9af
出典データセット
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05846942

反応ノート

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