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Lithium Hydroxide → 2-Isopropyl-5-(2-nitro-phenylamino)-thiazole-4-carboxylic acid ethyl ester

HRID 131361
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 131361
[CH2:1]([O:3][C:4]([C:6]1[N:7]=[C:8]([CH:12]([CH3:14])[CH3:13])[S:9][C:10]=1[NH2:11])=[O:5])[CH3:2].F[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[N+:22]([O-:24])=[O:23].[Li+].[OH-].C(O)(C(F)(F)F)=O>CS(C)=O.O.C(#N)C>[CH2:1]([O:3][C:4]([C:6]1[N:7]=[C:8]([CH:12]([CH3:13])[CH3:14])[S:9][C:10]=1[NH:11][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[N+:22]([O-:24])=[O:23])=[O:5])[CH3:2]
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Komponenten

8

Edukt 4

HCID 3939Lithium HydroxideHCID 6422Trifluoroacetic acidHCID 738951-Fluoro-2-nitrobenzeneHCID 58860584Ethyl 5-amino-2-isopropyl-1,3-thiazole-4-carboxylate

Produkt 1

HCID 588606132-Isopropyl-5-(2-nitro-phenylamino)-thiazole-4-carboxylic acid ethyl esterAusbeute 91,1 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 679Dimethyl SulfoxideLösungsmittel
HCID 962WaterLösungsmittel2×
HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

Combine a solution of 5-amino-2-isopropyl-thiazole-4-carboxylic acid ethyl ester (8.71 g, 40.6 mmol) and 2-fluoronitrobenzene (4.28 mL, 40.6 mmol) in DMSO (105 mL) and stir at rt under N2 as LiOH (1.95 g, 81.4 mmol, 2.0 eq.) or LiOH monohydrate (2 eq) is added in one portion. The reaction turns dark. Heat the reaction mixture to 55° C. for 3 h until complete by HPLC (Zorbax SB C18 25 cm, 60:40/ACN:0.1% TFA in water, 233 nm, 1.0 mL/min). Cool to rt overnight, Cool the reaction to 0-5° C. with stirring as deionized water (315 mL) is added at such a rate to maintain the temperature below 20° C. Precipitate the product and the reaction color changes from brown to rust-orange color. Stir the slurry for 3-4 h at rt, filter by vacuum and rinse with minimal 3:1/H2O:DMSO, dry in a vacuum oven at 60° C. to afford 12.4 g (91%) of the title compound as an orange solid: 1H NMR (300 MHz, DMSO-d6) δ 11.52 (bs, 1H), 8.23 (d, 1H, J=8.05 Hz), 7.80 (m, 2H), 7.21 (m, 1H), 4.36 (q, 2H, J=7.32 Hz, 6.95 Hz), 3.23 (dq, 1H, J=6.95 Hz), 1.34 (m, 9H); 13C NMR (75 MHz, DMSO-d6) δ 163.22, 161.85, 149.08, 136.99, 136.37, 136.10, 126.53, 126.48, 121.94, 117.05, 60.45, 32.47, 22.34(2), 14.24; IR (CHCl3) 2976, 2932, 2867, 1709, 1677, 1611, 1580, 1550, 1512, 1415, 1340 cm−; HRMS (ES) M/z calculated for C15H17N3O4S 336.1018, found 336.1009.

Aufarbeitung

  1. additionis added in one portion
  2. temperatureCool
  3. customthe reaction to 0-5° C.
  4. additionis added at such a rate
  5. temperatureto maintain the temperature below 20° C
  6. customPrecipitate the product
  7. filtrationfilter by vacuum
  8. washrinse with minimal 3:1/H2O
  9. dry with materialDMSO, dry in a vacuum oven at 60° C.

Quellen und Nachweise

ORD-Eintrag
ord-527e8196511f42098723af5df7ef2eb6
Quelldatensatz
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07384934B2

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