Methanol → methyl N-(2,6-dichlorobenzoyl)-4-iodo-L-phenylalaninate

HRID 1037817노트

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HRID 1037817 반응식
[CH3:1]O.S(=O)(=O)(O)O.[Cl:8][C:9]1[CH:29]=[CH:28][CH:27]=[C:26]([Cl:30])[C:10]=1[C:11]([NH:13][C@H:14]([C:23]([OH:25])=[O:24])[CH2:15][C:16]1[CH:21]=[CH:20][C:19]([I:22])=[CH:18][CH:17]=1)=[O:12]>O>[CH3:1][O:24][C:23](=[O:25])[C@H:14]([CH2:15][C:16]1[CH:17]=[CH:18][C:19]([I:22])=[CH:20][CH:21]=1)[NH:13][C:11](=[O:12])[C:10]1[C:9]([Cl:8])=[CH:29][CH:28]=[CH:27][C:26]=1[Cl:30]

참가 물질

5

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온도
40 °C

실험 절차

Methanol (40 mL) and 0.98 mL of concentrated sulfuric acid were added to 8.0 g of Nα-(2,6-dichlorobenzoyl)-4-iodo-L-phenylalanine and the reaction was carried out for 4 hours while heating the reaction system at 40° C. After confirming the completion of the reaction, the reaction system was cooled to 10° C. and 20 mL of water was dropwise added to separate out solid. The solid thus precipitated was isolated through filtration under reduced pressure, washed with 40 mL of water and then dried at 70° C. under reduced pressure to thus give 7.40 g of the desired product as a solid.

후처리

  1. customthe completion of the reaction
  2. temperaturethe reaction system was cooled to 10° C.
  3. customto separate out solid
  4. customThe solid thus precipitated
  5. customwas isolated through filtration under reduced pressure
  6. washwashed with 40 mL of water
  7. dry with materialdried at 70° C. under reduced pressure to thus give 7.40 g of the desired product as a solid

출처 및 근거

ORD 기록
ord-b6580e0b9fdd434fad8d5686965a6b2a
출처 데이터셋
uspto-grants-2013_10
특허 번호
US08546610B2

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