Sodium Hydroxide → Sodium 5-(4-{1-[({2,5-dimethyl-4-[4-(trifluoromethyl)benzyl]-3-thienyl}carbonyl)amino]cyclopropyl}phenyl)tetrazol-2-ide

HRID 870064Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 870064
[CH3:1][C:2]1[S:3][C:4]([CH3:35])=[C:5]([CH2:24][C:25]2[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:33])[F:32])=[CH:27][CH:26]=2)[C:6]=1[C:7]([NH:9][C:10]1([C:13]2[CH:18]=[CH:17][C:16]([C:19]3[N:20]=[N:21][NH:22][N:23]=3)=[CH:15][CH:14]=2)[CH2:12][CH2:11]1)=[O:8].[OH-].[Na+:37]>CCO>[CH3:1][C:2]1[S:3][C:4]([CH3:35])=[C:5]([CH2:24][C:25]2[CH:26]=[CH:27][C:28]([C:31]([F:34])([F:32])[F:33])=[CH:29][CH:30]=2)[C:6]=1[C:7]([NH:9][C:10]1([C:13]2[CH:18]=[CH:17][C:16]([C:19]3[N:20]=[N:21][N-:22][N:23]=3)=[CH:15][CH:14]=2)[CH2:11][CH2:12]1)=[O:8].[Na+:37]

Komponenten

4

Versuchsvorschrift

A suspension of 2,5-dimethyl-N-{1-[4-(2H-tetrazol-5-yl)phenyl]cyclopropyl}-4-[4-(trifluoromethyl)benzyl]thiophene-3-carboxamide from Example 14, Step 3 (150 mg, 0.301 mmol) in EtOH (3 mL), was treated with NaOH (1.0N in water, 301 μL, 0.301 mmol). The solution then obtained was concentrated to dryness. Water (20 mL) was added to the residue. The turbid solution was frozen in a bath of dry ice and acetone and lyophilized to afford the desired product as an off-white fluffy solid. MS (−APCI): m/z 496 (M−23)−.

Aufarbeitung

  1. customThe solution then obtained
  2. concentrationwas concentrated to dryness
  3. additionWater (20 mL) was added to the residue
  4. temperatureThe turbid solution was frozen in a bath of dry ice and acetone

Quellen und Nachweise

ORD-Eintrag
ord-4e69e387c7b644fc8251835c1433bd72
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08969394B2

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