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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Levodopa → Melevodopa

HRID 222813
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HRID 222813 반응식
[C:1](Cl)(=O)C.[CH:5]1[C:10]([CH2:11][C@H:12]([NH2:16])[C:13]([OH:15])=[O:14])=[CH:9][C:8]([OH:17])=[C:7]([OH:18])[CH:6]=1>CO>[CH3:1][O:14][C:13]([C@@H:12]([NH2:16])[CH2:11][C:10]1[CH:5]=[CH:6][C:7]([OH:18])=[C:8]([OH:17])[CH:9]=1)=[O:15]
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참가 물질

4

반응물 2

HCID 6047LevodopaHCID 6367Acetyl chloride

생성물 1

HCID 23497Melevodopa수율 117.3%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
15 °C

실험 절차

A 3-Liter three-necked round-bottom flask equipped with a cooling bath, a thermometer and a condenser was charged with 1.5 Liters methanol, and acetyl chloride (119 ml, 1.2 mol) was carefully added thereto at 0° C. The cooling bath was replaced with a heating mantle and the mixture was heated to 15° C. 60 grams (0.3 mol) of L-3-(3,4-dihydroxy-phenyl)alanine was then added and the reaction mixture was refluxed for 3 hours and thereafter concentrated under reduced pressure at 60° C. to afford 74.3 grams (100% yield) of Compound 2 (see, Scheme 1). The product structure was confirmed by 1H-NMR.

후처리

  1. customA 3-Liter three-necked round-bottom flask equipped with a cooling bath
  2. additionwas carefully added
  3. customat 0° C
  4. temperaturethe reaction mixture was refluxed for 3 hours
  5. concentrationconcentrated under reduced pressure at 60° C.

출처 및 근거

ORD 기록
ord-4a47b9208e444a0f9d11a7aa6fff6a61
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08207369B2

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