Triethylamine → Pyridine-2-carboxylic acid 4-(pyrrolidine-1-carbonyloxymethyl)-cyclohexyl ester

HRID 68484

反応式

HRID 68484 の反応式
[OH:1][CH:2]1[CH2:7][CH2:6][CH:5]([CH2:8][O:9][C:10]([N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)=[O:11])[CH2:4][CH2:3]1.[N:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[C:23](Cl)=[O:24].C(N(CC)CC)C>C(Cl)Cl.O>[N:12]1([C:10]([O:9][CH2:8][CH:5]2[CH2:6][CH2:7][CH:2]([O:1][C:23]([C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][N:17]=3)=[O:24])[CH2:3][CH2:4]2)=[O:11])[CH2:16][CH2:15][CH2:14][CH2:13]1

参加物

6

反応物 3

HCID 8471TriethylamineHCID 135034Pyridine-2-carbonyl chlorideHCID 66837799Pyrrolidine-1-carboxylic acid 4-hydroxycyclohexylmethyl ester

生成物 1

HCID 56952073Pyridine-2-carboxylic acid 4-(pyrrolidine-1-carbonyloxymethyl)-cyclohexyl ester収率 70.1%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒

実験手順

To a solution of pyrrolidine-1-carboxylic acid 4-hydroxy-cyclohexylmethyl ester (1 mmol) in methylene chloride (5 mL) were added picolinoyl chloride (1.1 mmol) and triethylamine (1.5 mmol) and the resulting mixture was stirred for 16 hours at room temperature. The reaction mixture was diluted with water, followed by few times of extraction with methylene chloride. The combined organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, ethyl acetate), thereby completing the preparation of a target compound (233 mg, 70% yield).

後処理

  1. extractionfollowed by few times of extraction with methylene chloride
  2. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by column chromatography (silica gel, ethyl acetate)

出典と根拠

ORDレコード
ord-cbcbb27e30584e42ab30cd8da7dcaf04
出典データセット
uspto-grants-2014_09
特許番号
US08822463B2

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