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2-(Methylthio)thiazole → HCID 178474897, Verbindung

HRID 2164984
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2164984
[CH2:1]([O:3]/[N:4]=[C:5](/[C:36]1[N:37]=[C:38]([NH:41]C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[S:39][CH:40]=1)\[C:6]([NH:8][CH:9]1[C:34](=[O:35])[N:11]2[C:12]([C:18]([O:20]C(C3C=CC=CC=3)C3C=CC=CC=3)=[O:19])=[C:13]([CH2:16]I)[CH2:14][S:15][C@H:10]12)=[O:7])[CH3:2].[CH3:61][S:62][C:63]1[S:64][CH:65]=[CH:66][N:67]=1>C(Cl)Cl.C(Cl)(Cl)Cl.[B-](F)(F)(F)F.[Ag+]>[NH2:41][C:38]1[S:39][CH:40]=[C:36](/[C:5](=[N:4]/[O:3][CH2:1][CH3:2])/[C:6]([NH:8][CH:9]2[C:34](=[O:35])[N:11]3[C:12]([C:18]([O-:20])=[O:19])=[C:13]([CH2:16][N+:67]4[CH:66]=[CH:65][S:64][C:63]=4[S:62][CH3:61])[CH2:14][S:15][C@H:10]23)=[O:7])[N:37]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 2

HCID 27601002-(Methylthio)thiazoleHCID 88600798benzhydryl (6R)-7-[[(2Z)-2-ethoxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino]-3-(iodomethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

Produkt 1

HCID 178474897HCID 178474897, VerbindungAusbeute 145,6 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 159722Silver tetrafluoroborateKatalysator
HCID 6212ChloroformLösungsmittel
HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To an ice-cooled solution of diphenylmethyl 7-[(Z)-2-(ethoxyimino)-2-(2-tritylaminothiazol-4-yl)acetamido]-3-iodomethyl-3-cephem-4-carboxylate [VII-2] (517 mg, 0.55 mmole) and 2-methylthiothiazole (85.3 mg, 0.65 mmole) in CH2Cl2 (10 ml) was added AgBF4 (117 mg, 0.60 mmole) and the mixture was stirred for 1.5 hours at room temperature. The reaction mixture was diluted with CHCl3 (100 mL), and the resulting precipitate was recovered by filtration and washed with CHCl3 (100 mL). The filtrate and the washings were combined and washed with water, dried over MgSO4 and evaporated. The residue was triturated with ether (50 mL) to give an amorphous solid (433 mg), which was dissolved in 90% TFA. The mixture was allowed to stand for 45 minutes at room temperature and then evaporated in vacuo at 10° C. The residue was triturated with ether to give crude Id (291 mg) which was dissolved in a small amount of methanol and passed through an HP-20 (20 mL) column by eluting with 30% aqueous methanol, to give 63.3 mg (29%) of the title compound [Id]. Estimated purity 70%.

Aufarbeitung

  1. filtrationthe resulting precipitate was recovered by filtration
  2. washwashed with CHCl3 (100 mL)
  3. washwashed with water
  4. dry with materialdried over MgSO4
  5. customevaporated
  6. customThe residue was triturated with ether (50 mL)

Quellen und Nachweise

ORD-Eintrag
ord-ce141a6285b94119995dcc3b02021cee
Quelldatensatz
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04507487

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