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

HRID 557453노트

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HRID 557453 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-7caa3274b13a427bb06c25b53eae78fe
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08058432B2

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