Water → HCID 54231516、化合物

HRID 1900186

反応式

HRID 1900186 の反応式
CN1CCOCC1.Cl[C:9]([O:11][CH:12]1[CH2:17][CH2:16][CH2:15][CH:14]([CH3:18])[CH2:13]1)=[O:10].[C:19]([C:21]1[CH:38]=[CH:37][C:24]([O:25][CH2:26][CH:27]([NH:29][C:30](=[O:36])[C@H:31]([CH:33]([CH3:35])[CH3:34])[NH2:32])[CH3:28])=[CH:23][CH:22]=1)#[N:20].O>C(Cl)Cl>[C:19]([C:21]1[CH:22]=[CH:23][C:24]([O:25][CH2:26][CH:27]([NH:29][C:30](=[O:36])[C@H:31]([CH:33]([CH3:34])[CH3:35])[NH:32][C:9]([O:11][CH:12]2[CH2:17][CH2:16][CH2:15][CH:14]([CH3:18])[CH2:13]2)=[O:10])[CH3:28])=[CH:37][CH:38]=1)#[N:20]

参加物

6

反応物 4

HCID 962WaterHCID 79724-MethylmorpholineHCID 127054633-Methylcyclohexyl chloroformateHCID 22866848N1-[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide

生成物 1

HCID 54231516HCID 54231516、化合物収率 79.5%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

0.4 g of N-methylmorpholine, and subsequently 0.8 g of 3-methylcyclohexyl chloroformate were added to a suspension containing 1.0 g of N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide suspended in 50 ml of methylene chloride at -15° C. The mixture was allowed to sit and warm naturally to room temperature and stirred for 15 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed with water, the organic layer was dried over anhydrous magnesium sulfate and then the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus obtaining 1.2 g of the desired product in the form of a white crystal (yield: 80% ).

後処理

  1. washAfter the methylene chloride layer was washed with water
  2. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  3. customthe methylene chloride was removed under reduced pressure
  4. customThe residue was purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-79bb7633d08d424ba82796a3a8d2600e
出典データセット
uspto-grants-1996_11
特許番号
US05574064

関連ノート

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