5-Aminovaleric acid → 4-(2-Oxopiperidinomethyl)-nitrobenzene

HRID 1374817

反応式

HRID 1374817 の反応式
[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[NH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=O.C([BH3-])#N.[Na+].Cl>CO.O>[O:19]=[C:17]1[CH2:16][CH2:15][CH2:14][CH2:13][N:12]1[CH2:8][C:7]1[CH:10]=[CH:11][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=1

参加物

7

反応物 4

HCID 1385-Aminovaleric acidHCID 313Hydrochloric AcidHCID 5414-NitrobenzaldehydeHCID 5003444Sodium cyanoborohydride

生成物 1

HCID 180056574-(2-Oxopiperidinomethyl)-nitrobenzene

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

6.4 g (42 mmol) of 4-nitrobenzaldehyde are dissolved in 150 ml of methanol and combined with 4.9 g (42 mmol) of 5-aminovaleric acid and 1.8 g (29 mmol) of sodium cyanoborohydride. The mixture is stirred for 18 hours at ambient temperature and then carefully mixed with 20 ml of conc. hydrochloric acid. The solvent is eliminated in vacuo, the residue is taken up in water and extracted with dichloromethane. The residue obtained after evaporation is chromatographed on silica gel (dichloromethane/methanol, 4:1). A mixture of methyl 5-(4-nitrobenzylamino)-pentanoate and 4-(2-oxopiperidinomethyl)-nitrobenzene is obtained which is dissolved in 100 methanol and combined with 50 ml of 1 N sodium hydroxide solution. The mixture is stirred for one hour at ambient temperature, 50 ml of 1 N hydrochloric acid are added and the reaction solution is evaporated down to 100 ml. The aqueous phase thus obtained is extracted with dichloromethane. The combined organic phases are dried over sodium sulphate and evaporated to dryness.

後処理

  1. extractionextracted with dichloromethane
  2. customThe residue obtained
  3. customafter evaporation
  4. customis chromatographed on silica gel (dichloromethane/methanol, 4:1)
  5. additionA mixture of methyl 5-(4-nitrobenzylamino)-pentanoate

出典と根拠

ORDレコード
ord-975a988f6a744c18ac49fa4ca54dbc0b
出典データセット
uspto-grants-2007_01
特許番号
US07166615B2

関連ノート

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