Anisole trifluoroacetic acid → HCID 178502773, Verbindung

HRID 329930Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 329930
[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:47]/[O:48][CH3:49])/[C:8]([NH:10][CH:11]2[C:45](=[O:46])[N:13]3[C:14]([C:42]([OH:44])=[O:43])=[C:15]([CH2:18][NH:19][C:20]4[N:21](C)[N:22]=[C:23](OC(C5C=CC=CC=5)C5C=CC=CC=5)[C:24](=[O:26])[N:25]=4)[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1.[C:50]1([O:56]C)C=CC=CC=1.C(O)(C(F)(F)F)=O>>[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:47]/[O:48][CH3:49])/[C:8]([NH:10][CH:11]2[C:45](=[O:46])[N:13]3[C:14]([C:42]([OH:44])=[O:43])=[C:15]([CH2:18][NH:19][C:20]4[NH:21][N:22]=[C:23]([CH2:50][OH:56])[C:24](=[O:26])[N:25]=4)[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1

Komponenten

3

Versuchsvorschrift

A solution of 7-[2-(2-aminothiazol-4-yl)-2-((Z)-methoxyimino)acetamido]-3-[(2,5-dihydro-6-diphenylmethoxy-2-methyl-5-oxo-1,2,4-triazin-3-yl)aminomethyl]ceph-3-em-4-carboxylic acid (400 mg.) in anisole/TFA (1:1 v/v; 10 ml.) was allowed to stand at ambient temperature for 20 minutes. The solvent was evaporated and the residue was dissolved in an aqueous ammonium carbonate buffer, pH6, and purified by HPLC using ammonium carbonate buffer/MeOH 92:8 v/v as eluant to give 7-[2-(2-aminothiazol-4-yl)-2-((Z)-methoxyimino)acetamido]-3-[(2,5-dihydro-6-hydroxymethyl-5-oxo-1,2,4-triazin-3-yl)aminomethyl]ceph-3-em-4-carboxylic acid (yield 25%) having the following nmr in solvent B:--3.52(s,3 H); 3.6(s, 2 H); 4.04(s, 3 H); 4.4(s, 2 H); 5.18(d,1 H); 5.84(d, 1 H); 7.1(s, 1 H).

Aufarbeitung

  1. customThe solvent was evaporated
  2. dissolutionthe residue was dissolved in an aqueous ammonium carbonate buffer, pH6
  3. custompurified by HPLC

Quellen und Nachweise

ORD-Eintrag
ord-6f57e2aaee6949b188c30940d487de51
Quelldatensatz
uspto-grants-1990_01
Patentnummer
US04894371

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