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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-butyl 2-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]-1,3-thiazole-5-carboxylate → tert-butyl 2-((R)-1-((S)-1,1-dimethylethylsulfinamido)ethyl)thiazole-5-carboxylate

HRID 1037981
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HRID 1037981 반응식
[C:1]([S@@:5](/[N:7]=[CH:8]/[C:9]1[S:10][C:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])=[CH:12][N:13]=1)=[O:6])([CH3:4])([CH3:3])[CH3:2].[CH3:21][Mg]Br>C(Cl)Cl>[CH3:2][C:1]([CH3:4])([S@@:5]([NH:7][C@@H:8]([C:9]1[S:10][C:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])=[CH:12][N:13]=1)[CH3:21])=[O:6])[CH3:3]
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4

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HCID 58418160tert-butyl 2-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]-1,3-thiazole-5-carboxylateHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 58418131tert-butyl 2-((R)-1-((S)-1,1-dimethylethylsulfinamido)ethyl)thiazole-5-carboxylate수율 64%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-70 °C

실험 절차

To a solution of (S,E)-tert-butyl 2-((tert-butylsulfinylimino)methyl)thiazole-5-carboxylate (15 g, 47 mmol) in DCM (500 mL) at −70° C. was slowly added methylmagnesium bromide (63 mL, 3 M in ether). The mixture was stirred at −70° C. for 3 h then quenched with sat. NH4Cl solution. The solution was then warmed to rt. After separation, the aqueous phase was extracted with DCM (3×200 mL). Combined organic phases were dried (Na2SO4), and concentrated. Flash column chromatography (DCM:MeOH, 100:0 to 100:1) afforded tert-butyl 2-((R)-1-((S)-1,1-dimethylethylsulfinamido)ethyl)thiazole-5-carboxylate (10 g, 64%). 1H NMR (CDCl3, 400 MHz) δ 8.14 (s, 1H), 4.76 (m, 1H), 4.15 (m, 1H), 1.60 (d, J=6.8 Hz, 3H), 1.50 (s, 9H), 1.20 (s, 9H).

후처리

  1. customat −70° C.
  2. customthen quenched with sat. NH4Cl solution
  3. temperatureThe solution was then warmed to rt
  4. customAfter separation
  5. extractionthe aqueous phase was extracted with DCM (3×200 mL)
  6. dry with materialCombined organic phases were dried (Na2SO4)
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f8ca441295ec430c895320e65bfc6908
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08546588B2

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