Hydrochloric Acid → H-Nva-Met-NH2.HCl

HRID 851723노트

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HRID 851723 반응식
[NH:1](C(OC(C)(C)C)=O)[C@H:2]([C:6]([NH:8][C@H:9]([C:14]([NH2:16])=[O:15])[CH2:10][CH2:11][S:12][CH3:13])=[O:7])[CH2:3][CH2:4][CH3:5].[ClH:24]>C(OCC)(=O)C.CCOCC>[NH2:1][C@H:2]([C:6]([NH:8][C@H:9]([C:14]([NH2:16])=[O:15])[CH2:10][CH2:11][S:12][CH3:13])=[O:7])[CH2:3][CH2:4][CH3:5].[ClH:24]

참가 물질

5

실험 절차

4.5 g (13 mmoles) of BOC-Nva-Met-NH2 are suspended in 20 ml of ethyl acetate, and 20 ml of a 6 n hydrochloric acid solution in ethyl acetate are added to the suspension. After one hour of standing the reaction mixture is diluted with ether, the separated precipitate is filtered off, and dried in vacuo over anhydrous sodium hydroxide. The resulting 4 g of crude product are recrystallized from a mixture of methanol and ether. 3.28 g (89%) of H-Nva-Met-NH2.HCl are obtained; m.p.: 198°-200° C., Rf5 =0.40, [α]D25 =+10.2° (c=1%, in methanol).

후처리

  1. filtrationthe separated precipitate is filtered off
  2. dry with materialdried in vacuo over anhydrous sodium hydroxide
  3. customThe resulting 4 g of crude product are recrystallized from a mixture of methanol and ether

출처 및 근거

ORD 기록
ord-76928549785c412ea2c9bc34b93953ca
출처 데이터셋
uspto-grants-1983_05
특허 번호
US04386073

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