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Triethylamine → HCID 66940370、化合物

HRID 1367898
ノート
印刷プレビュー

反応式

HRID 1367898 の反応式
[CH3:1][S:2][CH2:3][CH2:4][C:5](Cl)=[O:6].Cl.[CH3:9][O:10][C:11](=[O:21])[C@H:12]([CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[NH2:13].C(N(CC)CC)C>ClCCl>[CH3:9][O:10][C:11](=[O:21])[CH:12]([NH:13][C:5](=[O:6])[CH2:4][CH2:3][S:2][CH3:1])[CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 75736Methyl L-phenylalaninate hydrochlorideHCID 129214403-(Methylthio)propionyl Chloride

生成物 1

HCID 66940370HCID 66940370、化合物収率 92%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

1.556 g (11 mmol) of 3-methylsulfanyl-propionyl chloride was added slowly to a mixture of 2.20 g (10 mmol) of phenylalanine methyl ester hydrochloride, 4.18 mL (30 mmol) of triethyl amine and 50 mL of dichloromethane and stirred at room temperature for 2 h. The reaction mixture was partitioned between DCM (50 mL) and saturated NaHCO3 solution (100 mL). The aqueous layer was separated and extracted again with dichloromethane (100 mL). The combined organic extracts were dried over sodium sulfate and evaporated. Purification by column chromatography on silica gel gave 2.574 g (92%) of 2-(3-methylsulfanyl-propionylamino)-3-phenyl-propionic acid methyl ester. LCMS: 282 (M+1)+.

後処理

  1. customThe reaction mixture was partitioned between DCM (50 mL) and saturated NaHCO3 solution (100 mL)
  2. customThe aqueous layer was separated
  3. extractionextracted again with dichloromethane (100 mL)
  4. dry with materialThe combined organic extracts were dried over sodium sulfate
  5. customevaporated
  6. customPurification by column chromatography on silica gel

出典と根拠

ORDレコード
ord-7b6752022b4e44ada5109ecb5d45dba3
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07893267B2

反応ノート

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