N-{4-oxo-4-[3-(2-oxo-1-pyrrolidinyl)propylamino]butanoyl}-L-prolinol → N-{4-oxo-4-[3-(2-oxo-1-pyrrolidinyl)propylamino]butanoyl}-L-prolinal

HRID 892616ノート

反応式

HRID 892616 の反応式
[O:1]=[C:2]([NH:14][CH2:15][CH2:16][CH2:17][N:18]1[CH2:22][CH2:21][CH2:20][C:19]1=[O:23])[CH2:3][CH2:4][C:5]([N:7]1[CH2:13][CH2:12][CH2:11][C@H:8]1[CH2:9][OH:10])=[O:6]>C1C=CC=CC=1.CS(C)=O.C(N(CC)CC)C>[O:1]=[C:2]([NH:14][CH2:15][CH2:16][CH2:17][N:18]1[CH2:22][CH2:21][CH2:20][C:19]1=[O:23])[CH2:3][CH2:4][C:5]([N:7]1[CH2:13][CH2:12][CH2:11][C@H:8]1[CH:9]=[O:10])=[O:6]

参加物

5

反応物 1

HCID 54573583N-{4-oxo-4-[3-(2-oxo-1-pyrrolidinyl)propylamino]butanoyl}-L-prolinol

生成物 1

HCID 54280415N-{4-oxo-4-[3-(2-oxo-1-pyrrolidinyl)propylamino]butanoyl}-L-prolinal収率 65.1%

試薬・触媒・溶媒 3

HCID 241Benzene溶媒HCID 679Dimethyl Sulfoxide溶媒HCID 8471Triethylamine溶媒

実験手順

N-{4-Oxo-4-[3-(2-oxo-1-pyrrolidinyl)propylamino]butanoyl}-L-prolinol (85 mg) was dissolved in a mixed solvent of benzene (0.18 ml), DMSO (0.5 ml) and triethylamine (0.18 ml), and sulfur trioxide pyridine complex (200 mg) was added thereto under ice-cooling. After 1 hour's stirring at a temperature of 10°-15° C., the reaction mixture was treated in the same manner as in Example 10-C) to give 55 mg of N-{4-oxo-4-[3-(2-oxo-1-pyrrolidinyl)propylamino]butanoyl}-L-prolinal.

後処理

  1. additionwas added
  2. temperatureunder ice-cooling
  3. additionthe reaction mixture was treated in the same manner as in Example 10-C)

出典と根拠

ORDレコード
ord-6dd016ef147d4ebaa6e1a4b03a042aee
出典データセット
uspto-grants-1992_06
特許番号
US05118811

反応ノート

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