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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-{[5-(ethoxycarbonyl)-2-methyl-1,3-thiazol-4-yl]methyl}-1,4-oxazepane-4-carboxylate

HRID 1022711
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HRID 1022711 반응식
S(Cl)(Cl)(=O)=O.[Cl:6][C:7]1[CH:8]=[C:9]([C@@H:14]2[O:20][CH2:19][CH2:18][N:17]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:16][C@H:15]2[CH2:28][C:29](=O)[CH2:30][C:31]([O:33][CH2:34][CH3:35])=[O:32])[CH:10]=[CH:11][C:12]=1[Cl:13].[C:37]([NH2:40])(=[S:39])[CH3:38].C(N(CC)CC)C.C(OC(OC(C)(C)C)=O)(OC(C)(C)C)=O>C1(C)C=CC=CC=1.C(O)C>[Cl:6][C:7]1[CH:8]=[C:9]([C@@H:14]2[O:20][CH2:19][CH2:18][N:17]([C:21]([O:23][C:24]([CH3:25])([CH3:27])[CH3:26])=[O:22])[CH2:16][C@H:15]2[CH2:28][C:29]2[N:40]=[C:37]([CH3:38])[S:39][C:30]=2[C:31]([O:33][CH2:34][CH3:35])=[O:32])[CH:10]=[CH:11][C:12]=1[Cl:13]
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참가 물질

8

반응물 5

HCID 8471TriethylamineHCID 24648Sulfuryl chlorideHCID 90495Di-tert-butyl dicarbonateHCID 2723949ThioacetamideHCID 66976292tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-(4-ethoxy-2,4-dioxobutyl)-1,4-oxazepane-4-carboxylate

생성물 1

HCID 66975856
tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-{[5-(ethoxycarbonyl)-2-methyl-1,3-thiazol-4-yl]methyl}-1,4-oxazepane-4-carboxylate
수율 64.4%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 1140Toluene용매

실험 절차

Sulfuryl chloride (0.094 mL, 1.16 mmol) was added to a solution of tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-(4-ethoxy-2,4-dioxobutyl)-1,4-oxazepane-4-carboxylate (500 mg, 1.05 mmol) in toluene (5 mL). The reaction mixture was stirred at room temperature for 45 min, and concentrated under reduced pressure. To the residue were added ethanol (5 ml) and thioacetamide (87 mg, 1.16 mmol), and the mixture was stirred at 80° C. for 1.5 hr. To the reaction mixture were added triethylamine (0.294 mL, 2.11 mmol) and di-tert-butyl dicarbonate (0.291 ml, 1.26 mmol) at room temperature, and the mixture was stirred at room temperature for 30 min, and concentrated under reduced pressure. To the residue was added aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (358 mg).

후처리

  1. concentrationconcentrated under reduced pressure
  2. stirringthe mixture was stirred at 80° C. for 1.5 hr
  3. stirringthe mixture was stirred at room temperature for 30 min
  4. concentrationconcentrated under reduced pressure
  5. additionTo the residue was added aqueous sodium hydrogen carbonate solution
  6. extractionthe mixture was extracted with ethyl acetate
  7. washThe extract was washed with brine
  8. dry with materialdried over anhydrous sodium sulfate
  9. customThe solvent was evaporated under reduced pressure
  10. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-3c1529f8a629466da58cc58fcbddf0f7
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722662B2

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