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Toluene → 4-[[[1-(1,1-Dimethylethoxycarbonyl)-4-piperidinyl]amino]methyl]-3-(ethoxycarbonylamino)-thiophene

HRID 1699240
ノート
印刷プレビュー

反応式

HRID 1699240 の反応式
[CH2:1]([O:3][C:4]([NH:6][C:7]1[C:8]([CH:12]=O)=[CH:9][S:10][CH:11]=1)=[O:5])[CH3:2].[NH2:14][CH:15]1[CH2:20][CH2:19][N:18]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:17][CH2:16]1.C1(C)C=CC=CC=1.[BH4-].[Na+]>O>[CH3:26][C:24]([CH3:27])([O:23][C:21]([N:18]1[CH2:17][CH2:16][CH:15]([NH:14][CH2:12][C:8]2[C:7]([NH:6][C:4]([O:3][CH2:1][CH3:2])=[O:5])=[CH:11][S:10][CH:9]=2)[CH2:20][CH2:19]1)=[O:22])[CH3:25]
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 1140TolueneHCID 12682914-Amino-1-Boc-piperidineHCID 4311764Sodium borohydrideHCID 146721634-(Ethoxycarbonylamino)-thiophene-3-carboxaldehyde

生成物 1

HCID 183215714-[[[1-(1,1-Dimethylethoxycarbonyl)-4-piperidinyl]amino]methyl]-3-(ethoxycarbonylamino)-thiophene

試薬・触媒・溶媒 1

HCID 962
Water
溶媒
2 回

実験手順

A mixture of 28.2 g (0.142 mol) of 4-(ethoxycarbonyl-amino)-thiophene-3-carboxaldehyde, 28.2 g (0.141 mol) of 4-amino-1-(1,1-dimethyl-ethoxycarbonyl)piperidine and 300 ml of toluene was refluxed using a water separator until water formation had ceased. The solvent was removed in vacuo, the residue was dissolved in 300 ml of methanol and at room temperature combined batchwise with 5.5 g (0.145 mol) of sodium borohydride. The mixture was stirred for a further hour at room temperature, then evaporated down in vacuo and the residue was distributed between water and tert. butyl-methylether. The organic phase was dried over sodium sulphate and freed from solvent in vacuo. The oily residue was further processed without purification.

後処理

  1. temperaturewas refluxed
  2. customThe solvent was removed in vacuo
  3. dissolutionthe residue was dissolved in 300 ml of methanol and at room temperature
  4. customevaporated down in vacuo
  5. dry with materialThe organic phase was dried over sodium sulphate
  6. customThe oily residue was further processed without purification

出典と根拠

ORDレコード
ord-4bbacf1dfe1047e1b947bd3e96131dda
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06344449B1

反応ノート

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