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HCID 12736922, compound → HCID 12736925, compound

HRID 1833370
Notes
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Reaction equation

HRID 1833370 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:14][C:13]3[C:12](=[O:15])[C:11]([C:16]([O:18]CC)=[O:17])=[CH:10][NH:9][C:8]=3[C:7](=[O:21])[C:6]=2[CH:22]=1>Cl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:14][C:13]3[C:12](=[O:15])[C:11]([C:16]([OH:18])=[O:17])=[CH:10][NH:9][C:8]=3[C:7](=[O:21])[C:6]=2[CH:22]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 12736922HCID 12736922, compound

Product 1

HCID 12736925HCID 12736925, compoundYield 87.5%

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Procedure

A suspension of ethyl 8-chloro-4,10-dihydro-4,10-dioxo-1H-1-benzopyrano[3,2-b]pyridine-3-carboxylate (3.0 g, 0.0094 mole) in 6N hydrochloric acid (100 ml ) was refluxed under nitrogen for 15 hrs., cooled and filtered. The residue was washed with water and with acetone. Recrystallization from DMF gave white crystals (2.4 g, 87%), m.p. 325°-327°.

Workup

  1. temperaturewas refluxed under nitrogen for 15 hrs
  2. temperature, cooled
  3. filtrationfiltered
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
wash
The residue was washed with water and with acetone
  • customRecrystallization from DMF
  • Sources & evidence

    ORD record
    ord-15d3af4e6b18494ebd91db1be938a377
    Source dataset
    uspto-grants-1978_01
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04066655

    Reaction notes

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