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Sodium Methoxide → HCID 86658294, 화합물

HRID 74859
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HRID 74859 반응식
C([O:9][C@@H:10]1[C@@H:15]([O:16]C(=O)C2C=CC=CC=2)[C@H:14]([O:25]C(=O)C2C=CC=CC=2)[C@@H:13]([CH2:34][O:35]C(=O)C2C=CC=CC=2)[O:12][C@@H:11]1[O:44][C@@H:45]1[C@@H:50]([CH2:51][O:52]C(=O)C2C=CC=CC=2)[O:49][C@H:48]([O:61][C@@H:62]2[C@@H:100]([CH2:101][O:102]C(=O)C3C=CC=CC=3)[O:99][C@@H:65]([O:66][NH:67][C:68](=[O:98])[CH2:69][O:70][CH:71]3[CH2:95][CH2:94][C@@:93]4([CH3:96])[CH:73]([CH2:74][CH2:75][C@@H:76]5[C@@H:92]4[CH2:91][CH2:90][C@@:89]4([CH3:97])[C@H:77]5[CH2:78][CH2:79][C@@H:80]4[C@H:81]([CH3:88])[CH2:82][CH2:83][CH2:84][CH:85]([CH3:87])[CH3:86])[CH2:72]3)[C@H:64]([O:111]C(=O)C3C=CC=CC=3)[C@H:63]2[O:120]C(=O)C2C=CC=CC=2)[C@H:47]([O:129]C(=O)C2C=CC=CC=2)[C@H:46]1[O:138]C(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.C[O-].[Na+]>CO.C1COCC1>[C@H:11]1([O:44][C@@H:45]2[C@@H:50]([CH2:51][OH:52])[O:49][C@H:48]([O:61][C@@H:62]3[C@@H:100]([CH2:101][OH:102])[O:99][C@@H:65]([O:66][NH:67][C:68](=[O:98])[CH2:69][O:70][CH:71]4[CH2:95][CH2:94][C@@:93]5([CH3:96])[CH:73]([CH2:74][CH2:75][C@@H:76]6[C@@H:92]5[CH2:91][CH2:90][C@@:89]5([CH3:97])[C@H:77]6[CH2:78][CH2:79][C@@H:80]5[C@H:81]([CH3:88])[CH2:82][CH2:83][CH2:84][CH:85]([CH3:86])[CH3:87])[CH2:72]4)[C@H:64]([OH:111])[C@H:63]3[OH:120])[C@H:47]([OH:129])[C@H:46]2[OH:138])[O:12][C@H:13]([CH2:34][OH:35])[C@@H:14]([OH:25])[C@H:15]([OH:16])[C@H:10]1[OH:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 866582952-(Cholestan-3-yloxy)acetamido 2,3,4,6-tetra-O-benzoyl-alpha-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-alpha-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-beta-D-glucopyranoside

생성물 1

HCID 86658294HCID 86658294, 화합물수율 74.7%

시약·촉매·용매 1

HCID 21899815
MeOH tetrahydrofuran
용매

실험 절차

Amide 132 (345 mg, 175 μmol) was dissolved in MeOH/THF 1:1 (16 mL). NaOMe (500 μL of a 6M solution) was added and the solution was stirred at room temperature for 24 hrs. The mixture was neutralized with acidic resin and the solution filtered before the solvent was evaporated to yield the white solid product which was triturated with EtOAc and the solvent decanted (×3). The solid was dried under vacuum to yield 124 mg of the white solid product (76%) which was reacted on without further purification or characterisation.

후처리

  1. filtrationthe solution filtered before the solvent
  2. customwas evaporated
  3. customto yield the white solid product which
  4. customwas triturated with EtOAc
  5. customthe solvent decanted (×3)
  6. customThe solid was dried under vacuum

출처 및 근거

ORD 기록
ord-831aeb3b6144463aa88f1405cacc0b6c
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08828952B2

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