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1H-Pyrazole, 4-bromo-1-methyl- → 2-(Pyridin-3-ylmethyl)quinoxaline

HRID 2017269
Notes
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Reaction equation

HRID 2017269 reaction equation
C[n:1]1[n:4][cH:3][c:2](Br)c1.CO[c:5]1[c:10](OC)[c:9](OC)[cH:8][c:7](C(OCS([CH2:11][c:12]2[cH:17][n:16][cH:15][cH:14][cH:13]2)(=O)=O)=O)[cH:6]1>>[CH2:11]([c:2]1[n:1][c:9]([c:10]2[n:4][cH:3]1)[cH:8][cH:7][cH:6][cH:5]2)[c:12]3[cH:17][n:16][cH:15][cH:14][cH:13]3
ParticipantsConditionsSources & evidenceReaction notes

Participants

9

Reactant 2

HCID 1674331H-Pyrazole, 4-bromo-1-methyl-HCID 178492748HCID 178492748, compound

Product 1

HCID 1622658522-(Pyridin-3-ylmethyl)quinoxaline

Reagents, catalysts & solvents 6

HCID 516893Potassium BicarbonateReagentHCID 23683543Potassium t-amylateReagentHCID 111557942-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylCatalystHCID 178455864HCID 178455864, compoundCatalystHCID 312751,4-DioxaneSolventHCID 117669-PhenylanthraceneInternal standard

Conditions

Temperature
130 °C

Sources & evidence

ORD record
ord-2980332b4eea48af8c937e5e70722250
Source dataset
39k HTE dataset from Pfizer
DOI
10.1038/s41557
Original link
View source

Reaction notes

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On this pageParticipantsConditionsSources & evidenceReaction notes