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Hydrochloric Acid → N-Cbz-valylprolylglycine

HRID 886661
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HRID 886661 반응식
C[O:2][C:3](=[O:30])[CH2:4][NH:5][C:6](=[O:29])[C@@H:7]1[CH2:11][CH2:10][CH2:9][N:8]1[C:12](=[O:28])[C@H:13]([CH:25]([CH3:27])[CH3:26])[NH:14][C:15]([O:17][CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:16].[Li+].[OH-].Cl>C1COCC1>[C:15]([NH:14][C@H:13]([C:12]([N:8]1[CH2:9][CH2:10][CH2:11][C@H:7]1[C:6]([NH:5][CH2:4][C:3]([OH:30])=[O:2])=[O:29])=[O:28])[CH:25]([CH3:27])[CH3:26])([O:17][CH2:18][C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 67057640N-Cbz-valylprolylglycine methyl ester

생성물 1

HCID 67057723N-Cbz-valylprolylglycine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of N-Cbz-valylprolylglycine methyl ester (Cbz-NH-[VPG]-CO2CH3) (4.2 g, 10 mmol) in THF (20 mL) is added a 1M aqueous solution of LiOH (11 mL, 11 mmol) and the solution is stirred overnight. The resulting solution is acidified to pH about 7 with 1M HCl and the contents of the flask partitioned between water (30 mL) and ethyl acetate (30 mL). The organic phase is extracted with brine, dried over Na2SO4 then concentrated in vacuo to afford the desired compound.

후처리

  1. customthe contents of the flask partitioned between water (30 mL) and ethyl acetate (30 mL)
  2. extractionThe organic phase is extracted with brine
  3. dry with materialdried over Na2SO4
  4. concentrationthen concentrated in vacuo

출처 및 근거

ORD 기록
ord-60cc155b75f04da7a397973068d24126
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08246991B2

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