Hydrochloric Acid → HCID 15030109, compound
Reaction equation
[N:1]1N=N[N:4]2[CH:9]=[C:8]([CH:10]3[O:15][CH2:14][C:13](=[O:16])[N:12]([C:17]([CH3:20])([CH3:19])[CH3:18])[CH2:11]3)[CH:7]=[CH:6][C:5]=12.Cl[Sn]Cl.Cl>CO>[NH2:1][C:5]1[N:4]=[CH:9][C:8]([CH:10]2[O:15][CH2:14][C:13](=[O:16])[N:12]([C:17]([CH3:20])([CH3:19])[CH3:18])[CH2:11]2)=[CH:7][CH:6]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-(tetrazolo[1,5-a]pyrid-6-yl)-4-(1,1-dimethylethyl)-5-oxo-morpholine (550 mg), SnCl2 .2H2O (968 mg) and 0.2 ml of 12N hydrochloric acid in 60 ml of methanol was heated at reflux for 14.5 hours under nitrogen. The reaction mixture was concentrated under reduced pressure and then poured into ice water containing 5N sodium hydroxide. The basic aqueous mixture was repeatedly extracted with methylene chloride. The combined organic fractions were washed with water and saturated sodium chloride solution and then dried over anhydrous magnesium sulfate. Concentration gave 603 mg of crude product which was chromatographed on silica gel (95:5:1 methylene chloride:ethanol:ammonium hydroxide) to give 442 mg of product. Mass spectrum (FAB) 250 (M+1). 13C NMR (CDCl3) 27.9 49.5 57.7 69.2 74.3 108.5 123.6 135.8 146.3 158.7 167.4 ppm.
Workup
- temperatureat reflux for 14.5 hours under nitrogen
- concentrationThe reaction mixture was concentrated under reduced pressure
- additionpoured into ice water containing 5N sodium hydroxide
- extractionThe basic aqueous mixture was repeatedly extracted with methylene chloride
- washThe combined organic fractions were washed with water and saturated sodium chloride solution
- dry with materialdried over anhydrous magnesium sulfate
- concentrationConcentration
- customgave 603 mg of crude product which
- customwas chromatographed on silica gel (95:5:1 methylene chloride:ethanol:ammonium hydroxide)
Sources & evidence
- ORD record
- ord-cf1e529c7e4f4f7a998ef826381a262b
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05077290
Reaction notes
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