Boc-L-Valine → HCID 178448372, 화합물

HRID 1987708

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HRID 1987708 반응식
[CH3:1][CH:2]([C@H:4]([NH2:23])C([O:7][CH2:8][CH2:9][O:10][CH2:11][N:12]1[C:16]2[NH:17][C:18]([NH2:22])=[N:19][C:20](=[O:21])[C:15]=2[N:14]=[CH:13]1)=O)[CH3:3].[NH:24]([C:32]([O:34]C(C)(C)C)=O)[C@H:25]([C:29]([OH:31])=[O:30])[CH:26]([CH3:28])[CH3:27]>C(N(CC)CC)C>[CH:13]1[N:12]([CH2:11][O:10][CH2:9][CH2:8][OH:7])[C:16]2[N:17]=[C:18]([NH2:22])[N:19]=[C:20]([OH:21])[C:15]=2[N:14]=1.[CH3:1][CH:2]([C@H:4]([NH2:23])[C:32]([NH:24][C@H:25]([C:29]([OH:31])=[O:30])[CH:26]([CH3:27])[CH3:28])=[O:34])[CH3:3]

참가 물질

4

실험 절차

A mixture of Boc-Val and dicyclohexyl carbodiimide (DCC) in dimethylformamide (DMF) in a ratio of 1:2 DCC/Boc-Val was stirred for 1 hr at 0° C. under nitrogen atmosphere. A solution of acyclovir (1) and 4-N,N (dimethylamino)pyridine (DMAP) was added to the reaction mixture, stirred for 18 hrs and then filtered. The solvent of the filtrate was partially removed in vacuo and the impure solution was added dropwise to cold diethyl ether. The resulting precipitate (2) was filtered and dried, followed by acidolytic removal (treating Boc-Val-ACV with trifluoroacetic acid (TFA) for 30 min at 0° C.) of the Boc protecting group to yield Val-ACV (3). Compound (3) was neutralized by triethylamine (TEA) and treated with the amino acid anhydride of Boc-Val for about 5 hrs. The solvent was removed from the reaction mixture in vacuo and the reaction mixture was added dropwise to the cold diethyl ether. The resulting precipitate (4) was filtered, dried and the Boc group was deprotected (acidolytic removal) to yield the desired dipeptide ester of acyclovir Val-Val-ACV (5).

후처리

  1. customThe solvent was removed from the reaction mixture in vacuo
  2. additionthe reaction mixture was added dropwise to the cold diethyl ether
  3. filtrationThe resulting precipitate (4) was filtered
  4. customdried
  5. custom(acidolytic removal)

출처 및 근거

ORD 기록
ord-4e7d915a5562461fa8c3195f4a254656
출처 데이터셋
uspto-grants-2009_06
특허 번호
US07553812B2

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