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Methanol → (4-Pyrrolidin-1-yl-cyclohexyl)-methylamine

HRID 1819480
ノート
印刷プレビュー

反応式

HRID 1819480 の反応式
C(OC(=O)NC[CH:12]1[CH2:17][CH2:16][CH:15]([N:18]2[CH2:22][CH2:21][CH2:20][CH2:19]2)[CH2:14][CH2:13]1)C1C=CC=CC=1.C([O-])=O.[NH4+:27].[CH3:28]O>>[N:18]1([CH:15]2[CH2:14][CH2:13][CH:12]([NH:27][CH3:28])[CH2:17][CH2:16]2)[CH2:19][CH2:20][CH2:21][CH2:22]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

4

反応物 3

HCID 887MethanolHCID 2723923Ammonium formateHCID 69058995(4-Pyrrolidin-1-yl-cyclohexylmethyl)-carbamic acid benzyl ester

生成物 1

HCID 57457676(4-Pyrrolidin-1-yl-cyclohexyl)-methylamine

反応条件

温度
65 °C

実験手順

To a solution of (4-pyrrolidin-1-yl-cyclohexylmethyl)-carbamic acid benzyl ester (292 mg, 0.92 mmol) in MeOH (5 mL) was added ammonium formate (0.58 g, 9.20 mmol). The reaction flask was flushed with N2 prior to addition of 10% Pd/C (300 mg). The mixture was heated at 65° C. for 2 h whereupon TLC analysis (silica gel, 95:4.75:0.25 DCM/MeOH/NH4OH) showed complete consumption of 57. After cooling to room temperature the reaction mixture was filtered through a plug of celite in order to remove the Pd catalyst. The filtrate contained (4-pyrrolidin-1-yl-cyclohexyl)-methylamine which was used without further purification in the next step.

後処理

  1. customThe reaction flask was flushed with N2
  2. additionto addition of 10% Pd/C (300 mg)
  3. customconsumption of 57
  4. temperatureAfter cooling to room temperature the reaction mixture
  5. filtrationwas filtered through a plug of celite in order
  6. customto remove the Pd catalyst
  7. customwas used without further purification in the next step

出典と根拠

ORDレコード
ord-2fd31955a9b340e9906b9b2d6467a35c
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07601714B2

反応ノート

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