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Selenium → 7-Methoxy-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one

HRID 226265
Notes
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Reaction equation

HRID 226265 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH2:16][CH2:15][C:10]3=[N:11][CH:12]=[CH:13][CH:14]=[C:9]3[C:8](=[O:17])[C:7]=2[CH:18]=1.[Se]>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH:16]=[CH:15][C:10]3=[N:11][CH:12]=[CH:13][CH:14]=[C:9]3[C:8](=[O:17])[C:7]=2[CH:18]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 6326970SeleniumHCID 577544677-Methoxy-10,11-dihydro-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one

Product 1

HCID 577544317-Methoxy-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Conditions

Temperature
120 °C

Procedure

A mixture of 2.3 g (9.6 mmol) of the product from Example 23 step 4, 1.85 g (16.6 mmol) of selenium dioxyde and 5 ml of pyridine is stirred at 120° C. for 6 hr. The whole is poured into excess petroleum ether and the solution is evaporated giving 0.55 g (24%) of enough pure title product as to prosecute with the synthesis.

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

  1. customthe solution is evaporated

Sources & evidence

ORD record
ord-927970835fe54928acc167750afbfec8
Source dataset
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07557212B2

Reaction notes

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