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Sulfuric Acid → t-Butyl 7beta-amino-3-methyl-3-cephem-4-carboxylate

HRID 257806
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반응식

HRID 257806 반응식
[CH3:1][C:2]1[CH2:11][S:10][C@@H:5]2[C@H:6]([NH2:9])[C:7](=[O:8])[N:4]2[C:3]=1[C:12]([OH:14])=[O:13].S(=O)(=O)(O)O.[CH3:20][C:21](=[CH2:23])[CH3:22]>COCCOC>[NH2:9][C@@H:6]1[C:7](=[O:8])[N:4]2[C:3]([C:12]([O:14][C:21]([CH3:23])([CH3:22])[CH3:20])=[O:13])=[C:2]([CH3:1])[CH2:11][S:10][C@H:5]12
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참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 8255IsobutyleneHCID 334987-Aminodeacetoxycephalosporanic acid

생성물 1

HCID 10869362t-Butyl 7beta-amino-3-methyl-3-cephem-4-carboxylate수율 33.1%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

A mixture of 7-ADCA (10.0 g, 0.0467 mol), ethylene glycol dimethyl ether (80 ml), concentrated sulfuric acid (6.0 ml) and isobutylene (36.0 g, 0.6416 mol) in a pressure bottle was stirred at room temperature for 32 hours. Solvent was removed under reduced pressure. The residue was diluted with methylene chloride, washed with water, sodium bicarbonate solution, brine, dried over sodium sulfate and concentrated to give 4.18 g of t-butyl 7β-amino-3-methyl-3-cephem-4-carboxylate.

후처리

  1. customSolvent was removed under reduced pressure
  2. additionThe residue was diluted with methylene chloride
  3. washwashed with water, sodium bicarbonate solution, brine
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-38d72d0228a34655bc95aaf98572f87a
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05264430

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