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Sodium Methoxide → HCID 86658291, 화합물

HRID 74855
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HRID 74855 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:67]([CH2:68][O:69]C(=O)C3C=CC=CC=3)[O:66][C@H:65]([O:78][C@@H:79]3[C@@H:108]([CH2:109][O:110]C(=O)C4C=CC=CC=4)[O:107][C@@H:82]([O:83][CH2:84][CH2:85][CH2:86][NH:87][C:88](=[O:106])[CH2:89][CH2:90][CH2:91][CH2:92][CH2:93][CH2:94][CH2:95][CH2:96][CH2:97][CH2:98][CH2:99][CH2:100][CH2:101][CH2:102][CH2:103][CH2:104][CH3:105])[C@H:81]([O:119]C(=O)C4C=CC=CC=4)[C@H:80]3[O:128]C(=O)C3C=CC=CC=3)[C@H:64]([O:137]C(=O)C3C=CC=CC=3)[C@H:63]2[O:146]C(=O)C2C=CC=CC=2)[C@H:47]([O:155]C(=O)C2C=CC=CC=2)[C@H:46]1[O:164]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:67]([CH2:68][OH:69])[O:66][C@H:65]([O:78][C@@H:79]4[C@@H:108]([CH2:109][OH:110])[O:107][C@@H:82]([O:83][CH2:84][CH2:85][CH2:86][NH:87][C:88](=[O:106])[CH2:89][CH2:90][CH2:91][CH2:92][CH2:93][CH2:94][CH2:95][CH2:96][CH2:97][CH2:98][CH2:99][CH2:100][CH2:101][CH2:102][CH2:103][CH2:104][CH3:105])[C@H:81]([OH:119])[C@H:80]4[OH:128])[C@H:64]([OH:137])[C@H:63]3[OH:146])[C@H:47]([OH:155])[C@H:46]2[OH:164])[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 866582923-Stearamidopropyl 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-alpha-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-beta-D-glucopyranoside

생성물 1

HCID 86658291HCID 86658291, 화합물수율 99.7%

시약·촉매·용매 1

HCID 21899815
MeOH tetrahydrofuran
용매

실험 절차

Glycoside 126 (377 mg, 161 μmol) was dissolved in MeOH/THF 1:1 (10 mL). NaOMe (60 μL of an 11M 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 159 mg of the white solid product (quantitative) 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-da7c75efe12d4bef997b557cd751a63f
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08828952B2

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