Sodium Bicarbonate → HCID 20583279, compound
Reaction equation
[Cl:1][C:2]1[CH:21]=[CH:20][C:5]([CH2:6][NH:7][C:8]([C:10]2[CH:11]=[CH:12][C:13]3[S:17][CH:16]=[CH:15][C:14]=3[C:18]=2[OH:19])=[O:9])=[CH:4][CH:3]=1.[Cl-].[CH2:23]=[N+:24]1[CH2:29][CH2:28][O:27][CH2:26][CH2:25]1.C(=O)(O)[O-].[Na+]>C(#N)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][NH:7][C:8]([C:10]2[CH:11]=[CH:12][C:13]3[S:17][C:16]([CH2:23][N:24]4[CH2:29][CH2:28][O:27][CH2:26][CH2:25]4)=[CH:15][C:14]=3[C:18]=2[OH:19])=[O:9])=[CH:20][CH:21]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of N-(4-chlorobenzyl)-4-hydroxy-1-benzothiophene-5-carboxamide (Preparation 14, 0.15 g), 4-methylenemorpholin-4-ium chloride (0.13 g), and anhydrous acetonitrile (5 mL) is heated at reflux for 2 hours. Upon cooling, a saturated solution of sodium bicarbonate is added until the pH=9 and this solution is partitioned between ethyl acetate (50 mL) and water (50 mL). The organic layer is washed with brine, dried over Na2SO4, filtered, and concentrated to give a pink oil. Chromatography on a Biotage column eluting with 20% ethyl acetate in heptane (250 mL) and 50% ethyl acetate in heptane (500 mL) affords 140 mg (76%) of the title compound as a white solid. Physical characteristics: Mp 200° C.; MS (ESI+) for C21H21ClN2O3S m/z 417 (M+H)+.
Workup
- temperatureis heated
- temperatureat reflux for 2 hours
- temperatureUpon cooling
- customthis solution is partitioned between ethyl acetate (50 mL) and water (50 mL)
- washThe organic layer is washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customto give a pink oil
- washChromatography on a Biotage column eluting with 20% ethyl acetate in heptane (250 mL) and 50% ethyl acetate in heptane (500 mL)
Sources & evidence
- ORD record
- ord-fb1c393192af43838f51aa0c01258315
- Source dataset
- uspto-grants-2005_06
- Patent number
- US06903097B2
Reaction notes
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