Hydrochloric Acid → HCID 58897002, Verbindung

HRID 1409120Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1409120
[C:1]1([CH3:27])[CH:6]=[CH:5][C:4]([S:7]([N:10]2[C:14]3=[N:15][CH:16]=[CH:17][C:18]([C:19]4[CH:20]=[C:21]([CH2:25]O)[CH:22]=[CH:23][CH:24]=4)=[C:13]3[CH:12]=[CH:11]2)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[Li+].[OH-].[ClH:30]>C1COCC1.O>[Cl:30][CH2:25][C:21]1[CH:20]=[C:19]([C:18]2[CH:17]=[CH:16][N:15]=[C:14]3[N:10]([S:7]([C:4]4[CH:5]=[CH:6][C:1]([CH3:27])=[CH:2][CH:3]=4)(=[O:9])=[O:8])[CH:11]=[CH:12][C:13]=23)[CH:24]=[CH:23][CH:22]=1

Komponenten

6

Versuchsvorschrift

To a stirred solution of compound G″ in THF, water was added LiOH (3.68 g, 0.087 mol) at rt and stirred for 4 h at same temperature. The reaction mixture was concentrated to obtain residue which was diluted with water (50 ml), acidified with 2N aq. HCl solution, adjusted to pH=5-6, the precipitated solid was filtered, washed with water and dried (traces water were removed by co-evaporating with toluene) to obtain compound H″. The compound H″ was washed with diethyl ether to obtain desired purity.

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated
  2. customto obtain residue which
  3. filtrationthe precipitated solid was filtered
  4. washwashed with water
  5. customdried
  6. custom(traces water were removed by co-evaporating with toluene)

Quellen und Nachweise

ORD-Eintrag
ord-b511e69037344932a42fc6664733c342
Quelldatensatz
uspto-grants-2014_12
Patentnummer
US08921376B2

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