Boron trifluoride → 3-Allyloxymethyl-7-amino-ceph-3-eme-4-carboxylic acid

HRID 5158

반응식

HRID 5158 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)C=C>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])[CH:1]=[CH2:23]

참가 물질

5

반응물 3

HCID 6356Boron trifluorideHCID 7858Allyl AlcoholHCID 4413287-Aminocephalosporanic acid

생성물 1

HCID 1317167873-Allyloxymethyl-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 boron trifluoride, 136 ml of allyl alcohol and 115 ml of triethylamine were reacted and the 9 g of raw product was purified successively twice with hot hydrochloric acid and ammonium hydroxide to obtain 4.72 g of 3-allyloxymethyl-7-amino-ceph-3-eme-4-carboxylic acid.

후처리

  1. customwere reacted
  2. customthe 9 g of raw product was purified successively twice with hot hydrochloric acid and ammonium hydroxide

출처 및 근거

ORD 기록
ord-dcaa90fa626041689c210e2969f0e25b
출처 데이터셋
uspto-grants-1993_09
특허 번호
US05243043

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