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Sulfuric Acid → N-(benzyloxycarbonyl)-4-iodo-3-methyl-L-phenylalanine methyl ester

HRID 844874
ノート
印刷プレビュー

反応式

HRID 844874 の反応式
S(=O)(=O)(O)O.Cl.[CH3:7][O:8][C:9](=[O:31])[C@H:10]([CH2:22][C:23]1[CH:28]=[CH:27][C:26](N)=[C:25]([CH3:30])[CH:24]=1)[NH:11][C:12]([O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:13].N([O-])=O.[Na+].[I-:36].[K+]>O>[CH3:7][O:8][C:9](=[O:31])[C@H:10]([CH2:22][C:23]1[CH:28]=[CH:27][C:26]([I:36])=[C:25]([CH3:30])[CH:24]=1)[NH:11][C:12]([O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:13]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 1118Sulfuric AcidHCID 4875Potassium IodideHCID 23668193Sodium NitriteHCID 69336581n-(Benzyloxycarbonyl)-4-amino-3-methyl-l-phenylalanine methyl ester hydrochloride salt

生成物 1

HCID 69336706N-(benzyloxycarbonyl)-4-iodo-3-methyl-L-phenylalanine methyl ester収率 64%

試薬・触媒・溶媒 1

HCID 962
Water
溶媒
4 回

反応条件

温度
-1 °C

実験手順

A suspension of sulfuric acid (0.3 mL), water (36 mL) and N-(benzyloxycarbonyl)-4-amino-3-methyl-L-phenylalanine methyl ester hydrochloride salt (2.9 mmol, 1.1 g) was heated to obtain a clear solution. Then, it was cooled to −1° C. (ice-bath) and a solution of sodium nitrite (5.8 mmol, 400 mg) in water (8 mL) was added dropwise. The reaction mixture was stirred for 30 min, and a solution of potassium iodide (8.7 mmol, 1.5 g) in water (6 mL) was added to obtain a brown suspension. After stirring for 30 min, the reaction mixture was allowed to warm to room temperature and was stirred for 1 h. Then, the reaction mixture was diluted with water (100 mL) and was extracted with ethyl acetate (3×50 mL). The combined extracts were washed with saturated sodium bisulfite solution (100 mL) and brine solution (100 mL) and were dried over anhydrous magnesium sulfate. Filtration of the drying agent and concentration gave a crude product, which was purified by silica gel chromatography using a Biotage (40m) column to afford 0.84 g (64% yield) of N-(benzyloxycarbonyl)-4-iodo-3-methyl-L-phenylalanine methyl ester as an amorphous white solid. ES-HRMS m/e calcd for C19H20INO4 (M+Na) 476.0329, found 476.0336.

後処理

  1. temperaturewas heated
  2. customto obtain a clear solution
  3. customto obtain a brown suspension
  4. stirringAfter stirring for 30 min
  5. temperatureto warm to room temperature
  6. stirringwas stirred for 1 h
  7. extractionwas extracted with ethyl acetate (3×50 mL)
  8. washThe combined extracts were washed with saturated sodium bisulfite solution (100 mL) and brine solution (100 mL)
  9. dry with materialwere dried over anhydrous magnesium sulfate
  10. filtrationFiltration of the drying agent and concentration
  11. customgave a crude product, which
  12. customwas purified by silica gel chromatography

出典と根拠

ORDレコード
ord-1ba49bb172ec47318957736e1ff5ba73
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06380387B1

反応ノート

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