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Acetic Acid → HCID 178511784, 화합물

HRID 64839
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HRID 64839 반응식
C(OC([NH:11][C@H:12]([C:19]([N:21]1[CH2:34][CH2:33][CH2:32][C@H:22]1[C:23]([NH:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:24])=[O:20])[CH2:13][C:14]1[N:18]=[CH:17][NH:16][CH:15]=1)=O)C1C=CC=CC=1.Br.C(O)(=O)C>CCOCC>[NH2:11][C@H:12]([C:19]([N:21]1[CH2:34][CH2:33][CH2:32][C@H:22]1[C:23]([NH:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:24])=[O:20])[CH2:13][C:14]1[N:18]=[CH:17][NH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 260Hydrogen BromideHCID 178523864HCID 178523864, 화합물

생성물 1

HCID 178511784HCID 178511784, 화합물수율 161.4%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To 1.79 g of compound (95) was added 19 ml of 25% hydrobromic acid--acetic acid cooled in an ice bath followed by stirring one hour at room temperature. The reaction mixture was added to 190 ml of desiccator ether and precipitates thus formed were quickly collected by filtration and dried overnight in a desiccator containing potassium hydroxide to provide 2.05 g of L-histidyl-N-phenyl-L-prolinamide.2-hydrobromide (96).

후처리

  1. customprecipitates thus
  2. customformed
  3. filtrationwere quickly collected by filtration
  4. customdried overnight in a desiccator
  5. additioncontaining potassium hydroxide

출처 및 근거

ORD 기록
ord-71061dfacf2b46fa892634dba8e1b2cb
출처 데이터셋
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04610821

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