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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Propanol → 3-Propoxymethyl-7-amino-ceph-3-eme-4-carboxylic acid

HRID 5159
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반응식

HRID 5159 반응식
[CH3:1][C:2]([O:4][CH2:5][C:6]1[CH2:15][S:14][C@@H:9]2[C@H:10]([NH2:13])[C:11](=[O:12])[N:8]2[C:7]=1[C:16]([OH:18])=[O:17])=O.B(F)(F)F.[CH2:23](O)CC>C(N(CC)CC)C>[CH2:2]([O:4][CH2:5][C:6]1[CH2:15][S:14][C@@H:9]2[CH:10]([NH2:13])[C:11](=[O:12])[N:8]2[C:7]=1[C:16]([OH:18])=[O:17])[CH2:1][CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10311-PropanolHCID 6356Boron trifluorideHCID 4413287-Aminocephalosporanic acid

생성물 1

HCID 1317167883-Propoxymethyl-7-amino-ceph-3-eme-4-carboxylic acid

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

Using the procedure of Step A of Example 8, 27.2 g of 7-amino-cephalosporanic acid, 170 ml of the etherate of of boron trifluoride, 131 ml of propanol and 128 ml of triethylamine were reacted to obtain 17.4 g of raw product which was purified with hot hydrochloric acid and ammonium hydroxide to obtain 7.45 g of 3-propoxymethyl-7-amino-ceph-3-eme-4-carboxylic acid.

후처리

  1. customwere reacted
  2. customto obtain 17.4 g of raw product which
  3. customwas purified with hot hydrochloric acid and ammonium hydroxide

출처 및 근거

ORD 기록
ord-332c42f9e23541eaa37b1a643ef16125
출처 데이터셋
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05243043

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