홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Hydrochloric Acid → HCID 178512901, 화합물

HRID 1414682
노트
인쇄 미리보기

반응식

HRID 1414682 반응식
[NH:1](C(OCC1C=CC=CC=1)=O)[C@H:2]([C:13]([N:15]1[CH2:56][CH2:55][CH2:54][C@H:16]1[C:17]([NH:19][C@H:20]([C:28]([NH:30][C@H:31]([C:39]([NH:41][C@H:42]([C:51]([NH2:53])=[O:52])[CH2:43][C:44]1[CH:49]=[CH:48][C:47]([OH:50])=[CH:46][CH:45]=1)=[O:40])[CH2:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=[O:29])[CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:18])=[O:14])[CH2:3][CH2:4][CH2:5][NH:6][C:7](=[NH:12])[NH:8][N+]([O-])=O.Cl.N[C@H](C(O)=O)CCCNC(=N)N.N[C@H](C(O)=O)CC1C=CC(O)=CC=1.N[C@H](C(O)=O)CC1C=CC=CC=1>[Pd].O.C(O)(=O)C>[NH2:1][C@H:2]([C:13]([N:15]1[CH2:56][CH2:55][CH2:54][C@H:16]1[C:17]([NH:19][C@H:20]([C:28]([NH:30][C@H:31]([C:39]([NH:41][C@H:42]([C:51]([NH2:53])=[O:52])[CH2:43][C:44]1[CH:49]=[CH:48][C:47]([OH:50])=[CH:46][CH:45]=1)=[O:40])[CH2:32][C:33]1[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=1)=[O:29])[CH2:21][C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1)=[O:18])=[O:14])[CH2:3][CH2:4][CH2:5][NH:6][C:7](=[NH:8])[NH2:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 5

HCID 313Hydrochloric AcidHCID 6057L-TyrosineHCID 6140L-PhenylalanineHCID 178418600HCID 178418600, 화합물HCID 178512178HCID 178512178, 화합물

생성물 1

HCID 178512901HCID 178512901, 화합물

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 176Acetic Acid용매HCID 962Water용매

실험 절차

In 30 ml. of acetic acid was dissolved 500 mg. of Z-Arg(NO2)-Pro-Phe-Phe-Tyr-NH2, and catalytic reduction was carried out with Pd-black as a catalyst for 20 hours. The catalyst was filtered off and the filtrate was concentrated to dryness under reduced pressure. The residue was dissolved in 50 ml. of water and, after the small amounts of insolubles were filtered off, the filtrate was lyophilized. The product was dissolved in 5 ml. of water and the solution was applied on a column (1.8 × 9 cm) of carboxymethyl-sephadex. Gradient elution was carried out with 0.1M aqueous ammonium acetate (400 ml.) and 1M aqueous ammonium acetate (400 ml.). The fractions from 250 ml. to 370 ml. were pooled and lyophilized to yield 250 mg. (52.3 %) of a white fluffy product. [α]D24 -41.9° (c=0.47 %, water). Amino acid analysis (hydrolysis with HCl): Arg, 1.00;Pro, 1.05; Tyr, 0.91; Phe, 1.96;(peptide content 86.5 %).

후처리

  1. filtrationThe catalyst was filtered off
  2. concentrationthe filtrate was concentrated to dryness under reduced pressure
  3. dissolutionThe residue was dissolved in 50 ml
  4. filtrationof water and, after the small amounts of insolubles were filtered off
  5. dissolutionThe product was dissolved in 5 ml
  6. washGradient elution
  7. customto yield 250 mg

출처 및 근거

ORD 기록
ord-68c06e1ab20c47c3aea036b125c822ac
출처 데이터셋
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04001199

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트