(1S)-1,5-anhydro-2,3,4,6-tetra-O-benzyl-1-[2-(benzyloxy)-5-[4-[2-[[[(2-hydroxy-1,1-dimethylethyl)amino]carbonyl]amino]ethyl]benzyl]-4-methylphenyl)-D-glucitol → (1S)-1,5-anhydro-1-[5-[4-[2-[[(2-hydroxy-1,1-dimethylethyl)aminocarbonyl]amino]ethyl]benzyl]-2-hydroxy-4-methylphenyl]-D-glucitol

HRID 1009890노트

반응식

HRID 1009890 반응식
C([O:8][C@@H:9]1[C@@H:14]([O:15]CC2C=CC=CC=2)[C@H:13]([O:23]CC2C=CC=CC=2)[C@@H:12]([CH2:31][O:32]CC2C=CC=CC=2)[O:11][C@H:10]1[C:40]1[CH:45]=[C:44]([CH2:46][C:47]2[CH:52]=[CH:51][C:50]([CH2:53][CH2:54][NH:55][C:56]([NH:58][C:59]([CH3:63])([CH3:62])[CH2:60][OH:61])=[O:57])=[CH:49][CH:48]=2)[C:43]([CH3:64])=[CH:42][C:41]=1[O:65]CC1C=CC=CC=1)C1C=CC=CC=1>[OH-].[Pd+2].[OH-].CO>[OH:61][CH2:60][C:59]([NH:58][C:56]([NH:55][CH2:54][CH2:53][C:50]1[CH:51]=[CH:52][C:47]([CH2:46][C:44]2[C:43]([CH3:64])=[CH:42][C:41]([OH:65])=[C:40]([C@@H:10]3[O:11][C@H:12]([CH2:31][OH:32])[C@@H:13]([OH:23])[C@H:14]([OH:15])[C@H:9]3[OH:8])[CH:45]=2)=[CH:48][CH:49]=1)=[O:57])([CH3:62])[CH3:63]

참가 물질

4

실험 절차

To a methanol solution (4 mL) of (1S)-1,5-anhydro-2,3,4,6-tetra-O-benzyl-1-[2-(benzyloxy)-5-[4-[2-[[[(2-hydroxy-1,1-dimethylethyl)amino]carbonyl]amino]ethyl]benzyl]-4-methylphenyl]-D-glucitol (0.184 mg, 0.190 mmol) was added 20% palladium hydroxide (0.180 g), and the mixture was stirred under a hydrogen atmosphere at room temperature overnight. The reaction solution was filtered through celite and evaporated under reduced pressure. Thus obtained residue was purified with silica gel column chromatography (chloroform:methanol=17:3) to obtain the title compound (57 mg, 58%) as a colorless powder. NMR data and MS data of the compound are shown in Table 1.

후처리

  1. filtrationThe reaction solution was filtered through celite
  2. customevaporated under reduced pressure
  3. customThus obtained residue was purified with silica gel column chromatography (chloroform:methanol=17:3)

출처 및 근거

ORD 기록
ord-77ec8803dd5d4dc1aee73390bd751539
출처 데이터셋
uspto-grants-2011_07
특허 번호
US07973012B2

반응 노트

불러오는 중…