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Hydrochloric Acid → Ethyl 2-[(2-hydroxy-4-{[5-(methylsulfonyl)pyridin-2-yl]oxy}phenyl)hydrazono]propanoate

HRID 1188919
Notes
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Reaction equation

HRID 1188919 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]2[CH:14]=[CH:13][C:12]([S:15]([CH3:18])(=[O:17])=[O:16])=[CH:11][N:10]=2)=[CH:4][C:3]=1[OH:19].Cl.[N:21]([O-])=O.[Na+].[CH3:25][CH:26](C(=O)C)[C:27]([O:29][CH2:30][CH3:31])=[O:28].[OH-].[K+]>C(O)C.C(#N)C.O.C(OCC)(=O)C>[OH:19][C:3]1[CH:4]=[C:5]([O:8][C:9]2[CH:14]=[CH:13][C:12]([S:15]([CH3:18])(=[O:17])=[O:16])=[CH:11][N:10]=2)[CH:6]=[CH:7][C:2]=1[NH:1][N:21]=[C:26]([CH3:25])[C:27]([O:29][CH2:30][CH3:31])=[O:28]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

10

Reactant 5

HCID 313Hydrochloric Acid2×HCID 701Ethyl 2-methylacetoacetateHCID 14797Potassium HydroxideHCID 23668193Sodium NitriteHCID 671184982-Amino-5-{[5-(methylsulfonyl)pyridin-2-yl]oxy}phenol

Product 1

HCID 86652844
Ethyl 2-[(2-hydroxy-4-{[5-(methylsulfonyl)pyridin-2-yl]oxy}phenyl)hydrazono]propanoate

Reagents, catalysts & solvents 4

HCID 702EthanolSolvent2×HCID 962WaterSolvent3×HCID 6342AcetonitrileSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
-5 °C

Procedure

To a stirring suspension of 2-amino-5-{[5-(methylsulfonyl)pyridin-2-yl]oxy}phenol (27.68 g) in a mixture of ethanol (150 mL) and acetonitrile (20 mL) was added concentrated hydrochloric acid (21.8 mL) at 0° C. After cooling to −5° C., a solution of sodium nitrite (8.18 g) in water (20 mL) was added dropwise to the mixture with keeping the temperature below −5° C. The mixture was stirred at −10° C. for 30 min. The mixture was added to a mixture of ethyl 2-methyl-3-oxobutanoate (15.7 mL), potassium hydroxide (85%, 22.8 g), ethanol (50 mL) and water (150 mL) at −30 to −20° C. After stirring at −30° C. for 1 h, 1M hydrochloric acid (150 mL) was added to the mixture. Water and ethyl acetate were added. The resulting brown suspension was filtered to give the title compound (17.9 g) as a brown solid. Furthermore, the filtrate was extracted with ethyl acetate-tetrahydrofuran. The organic layer was washed with saturated brine, dried over magnesium sulfate, filtered and concentrated. The residual solid was washed with diethyl ether to give the title compound (15.3 g) as a brownish solid. Additionally, the filtrate was concentrated and the residual solid was washed with diethyl ether to give the title compound (4.5 g) as a brownish solid (total 37.7 g, 97%). MS 394 (MH+).

Workup

  1. customthe temperature below −5° C
  2. stirringAfter stirring at −30° C. for 1 h
  3. filtrationThe resulting brown suspension was filtered

Sources & evidence

ORD record
ord-d7a244ecd3824b19951d0e346804f0c3
Source dataset
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08673942B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes