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Hydrochloric Acid → 2-(2-oxo-3,4-dihydro-1,6-naphthyridin-1(2H)-yl)acetic acid

HRID 1519903
Notes
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Reaction equation

HRID 1519903 reaction equation
Cl.[O:2]=[C:3]1[CH2:12][CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[N:8][CH:9]=2)[N:4]1[CH2:13][C:14]([O:16]C)=[O:15]>C(O)(=O)C>[O:2]=[C:3]1[CH2:12][CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[N:8][CH:9]=2)[N:4]1[CH2:13][C:14]([OH:16])=[O:15]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 68782506methyl 2-(2-oxo-3,4-dihydro-1,6-naphthyridin-1(2H)-yl)acetate

Product 1

HCID 687868432-(2-oxo-3,4-dihydro-1,6-naphthyridin-1(2H)-yl)acetic acid

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Conditions

Temperature
60 °C

Procedure

Aqueous 1N HCl (2 mL) was added to a solution of methyl 2-(2-oxo-3,4-dihydro-1,6-naphthyridin-1(2H)-yl)acetate (1.24 g, 5.67 mmol) in acetic acid (5 mL) and the resulting mixture was heated to 60° C. for 4 h. The solution was concentrated under vacuum to give 2-(2-Oxo-3,4-dihydro-1,6-naphthyridin-1(2H)-yl)acetic acid. Retention time (min)=0.275, method [1], MS(ESI) 207.0 (M+H).

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

  1. concentrationThe solution was concentrated under vacuum

Sources & evidence

ORD record
ord-03239bf592de43ac8f998c88cc38d75f
Source dataset
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09073891B2

Reaction notes

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