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2-Bromoquinoxaline → HCID 178480192, compound

HRID 2017234
Notes
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Reaction equation

HRID 2017234 reaction equation
COc1c(OC)c(OC)cc(C(OCS([CH2:1][c:2]2[cH:7][n:6][cH:5][cH:4][cH:3]2)(=O)=O)=O)c1.Brc1[n:13][c:12]([c:10]2[n:9][cH:8]1)[cH:11]ccc2>>[CH3:8][n:9]1[n:13][cH:11][c:12]([CH2:1][c:2]2[cH:7][n:6][cH:5][cH:4][cH:3]2)[cH:10]1
ParticipantsConditionsSources & evidenceReaction notes

Participants

9

Reactant 2

HCID 5822252-BromoquinoxalineHCID 178492748HCID 178492748, compound

Product 1

HCID 178480192HCID 178480192, compound

Reagents, catalysts & solvents 6

HCID 516893Potassium BicarbonateReagentHCID 23683543Potassium t-amylateReagentHCID 16217916Dicyclohexyl(2,4,6-trimethylphenyl)phosphaneCatalystHCID 178455864HCID 178455864, compoundCatalystHCID 312751,4-DioxaneSolventHCID 117669-PhenylanthraceneInternal standard

Conditions

Temperature
130 °C

Sources & evidence

ORD record
ord-52df5cc1d41445f9a6d39c5e3bc3b073
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