Tetrahydrofuran → 3-Hydroxymethyl-beta-carboline

HRID 574128ノート

反応式

HRID 574128 の反応式
[C:1]([C:5]1[N:6]=[CH:7][C:8]2[NH:9][C:10]3[C:15]([C:16]=2[CH:17]=1)=[CH:14][CH:13]=[CH:12][CH:11]=3)(OC)=[O:2].C1COCC1.[BH4-].[Na+]>O>[OH:2][CH2:1][C:5]1[N:6]=[CH:7][C:8]2[NH:9][C:10]3[C:15]([C:16]=2[CH:17]=1)=[CH:14][CH:13]=[CH:12][CH:11]=3

参加物

5

反応物 3

HCID 8028TetrahydrofuranHCID 107704Methyl 9H-pyrido(3,4-b)indole-3-carboxylateHCID 4311764Sodium borohydride

生成物 1

HCID 53533383-Hydroxymethyl-beta-carboline

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

3-carbomethoxy-β-carboline or a derivative thereof (J in Scheme VII above) is dissolved in a polar solvent (e.g., THF), and a reducing agent (e.g., NaBH4) is added to the solution. The mixture is stirred for a few hours and cooled. An excess of water is then added, and the mixture is stirred for another few hours. The solvent is thereafter evaporated and the resulting residue is dissolved in water, washed several times with one or more non-polar solvents such as dichloromethane and ethyl acetate, and the combined organic extracts are then evaporated. The remaining residue is purified by column chromatography (e.g., on a silica gel with elution by a 9:1 mixture of ethylacetate and methanol), to give a 3-hydroxymethyl-β-carboline intermediate.

後処理

  1. temperaturecooled
  2. stirringthe mixture is stirred for another few hours
  3. customThe solvent is thereafter evaporated
  4. dissolutionthe resulting residue is dissolved in water
  5. washwashed several times with one or more non-polar solvents such as dichloromethane and ethyl acetate
  6. customthe combined organic extracts are then evaporated
  7. customThe remaining residue is purified by column chromatography (e.g.
  8. washon a silica gel with elution
  9. additionby a 9:1 mixture of ethylacetate and methanol),

出典と根拠

ORDレコード
ord-ec33a9ffa6874c778560b7e2fa43f17d
出典データセット
uspto-grants-2015_05
特許番号
US09034872B2

反応ノート

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