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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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L-Methionine → Cbz-L-methionine methyl ester

HRID 58387
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HRID 58387 반응식
[NH2:1][C@H:2]([C:7]([OH:9])=[O:8])[CH2:3][CH2:4][S:5][CH3:6].[C:10](=O)(O)O.[Na].Cl[C:16]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17]>CCOC(C)=O.O>[CH3:10][O:8][C:7](=[O:9])[C@@H:2]([NH:1][C:16]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17])[CH2:3][CH2:4][S:5][CH3:6]
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참가 물질

6

반응물 3

HCID 6137L-MethionineHCID 10387Benzyl chloroformateHCID 24192197Carbonic acid, sodium salt

생성물 1

HCID 11141035Cbz-L-methionine methyl ester

시약·촉매·용매 2

HCID 962Water용매HCID 8857Ethyl Acetate용매

실험 절차

L-methionine (3.70 g, 18.5 mmol) was dissolved in a biphasic mixture of EtOAc (75 mL) and water (75 mL). This was cooled in ice and sodium hydrogen bicarbonate (7.78 g, 5 equiv) and benzyl chloroformate (2.98 mL, 1.1 equiv) were added. This was stirred in ice for one h′ and then at rt for a further eighteen h before the mixture was allowed to partition. The organic phase was washed sequentially with 1M hydrochloric acid, saturated aqueous sodium hydrogen bicarbonate and brine before being dried (MgSO4), filtered and concentrated in vacuo to afford a yellow oil, 5.40 g, 98%.

후처리

  1. temperatureThis was cooled in ice
  2. customto partition
  3. washThe organic phase was washed sequentially with 1M hydrochloric acid, saturated aqueous sodium hydrogen bicarbonate and brine
  4. dry with materialbefore being dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto afford a yellow oil, 5.40 g, 98%

출처 및 근거

ORD 기록
ord-5cb80fc450934bafb6832fa71e00a402
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434762B2

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