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tert-butyl N-methyl-N-(3-oxopropyl)carbamate → Tert-butyl 3-(4-(dimethylamino)-4-phenylpiperidin-1-yl)propyl(methyl)carbamate

HRID 453896
ノート
印刷プレビュー

反応式

HRID 453896 の反応式
[CH3:1][N:2]([CH2:10][CH2:11][CH:12]=O)[C:3](=[O:9])[O:4][C:5]([CH3:8])([CH3:7])[CH3:6].Cl.Cl.[CH3:16][N:17]([CH3:30])[C:18]1([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]1.C(B)#N.[Na]>CO.C(O)(=O)C.CO.C(Cl)(Cl)Cl>[CH3:16][N:17]([CH3:30])[C:18]1([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH2:19][CH2:20][N:21]([CH2:12][CH2:11][CH2:10][N:2]([CH3:1])[C:3](=[O:9])[O:4][C:5]([CH3:8])([CH3:7])[CH3:6])[CH2:22][CH2:23]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 10442454tert-butyl N-methyl-N-(3-oxopropyl)carbamateHCID 67366566N,N-dimethyl-4-phenylpiperidin-4-amine dihydrochlorideHCID 101953985CID 1019539852 回

生成物 1

HCID 68494485Tert-butyl 3-(4-(dimethylamino)-4-phenylpiperidin-1-yl)propyl(methyl)carbamate収率 60.4%

試薬・触媒・溶媒 3

HCID 176Acetic Acid溶媒
2 回
HCID 887Methanol溶媒
HCID 21584188Chloroform methanol溶媒

反応条件

温度
0 °C

実験手順

11.1 g (1.3 eq.) tert-butyl methyl(3-oxopropyl)carbamate were added to a solution of 11 g (1 eq.) N,N-dimethyl-4-phenylpiperidin-4-amine dihydrochloride in 110 ml methanol at 0° C. and the reaction mixture was stirred for 15 min at 0° C. 6.2 g (3 eq.) sodium cyanoboron hydride were then added in portions and the mixture was stirred for 30 min at room temperature. The reaction mixture obtained was adjusted to a pH of 5-6 with acetic acid and stirred for 12 h at room temperature. The reaction course was monitored by thin-layer chromatography (20% MeOH/CHCl3). As the conversion was still not complete, 2.4 g sodium cyanoboron hydride were added and the reaction mixture obtained was adjusted to pH 5-6 with acetic acid and stirred for 60 min at room temperature. Once the conversion was complete, the methanol was distilled off, the mixture was made alkaline with saturated NaHCO3 solution, the mixture obtained was extracted with chloroform (3×100 ml) and the combined organic phases were dried over Na2SO4. Following removal of the solvent under reduced pressure, the residue was purified by column chromatography (silica gel; 5% MeOH/CHCl3). 9 g (60%) of product were obtained.

後処理

  1. stirringthe mixture was stirred for 30 min at room temperature
  2. customThe reaction mixture obtained
  3. stirringstirred for 12 h at room temperature
  4. customthe reaction mixture obtained
  5. stirringstirred for 60 min at room temperature
  6. distillationthe methanol was distilled off
  7. customthe mixture obtained
  8. extractionwas extracted with chloroform (3×100 ml)
  9. dry with materialthe combined organic phases were dried over Na2SO4
  10. customremoval of the solvent under reduced pressure
  11. customthe residue was purified by column chromatography (silica gel; 5% MeOH/CHCl3)

出典と根拠

ORDレコード
ord-1dc9030852d44bd5a14d9547d94dfdd9
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08492559B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート