6-Bromoindole → HCID 178527351, compound

HRID 1938007Notes

Reaction equation

HRID 1938007 reaction equation
Brc1ccc2cc[nH]c2c1.CC1(C)OB(c2ccc(N3CCN(S(=O)(=O)c4ccc(Cl)cc4)CC3)nc2)OC1(C)C>COCCOC.O.O=C([O-])[O-].[CH]1[CH][CH]C(P(c2ccccc2)c2ccccc2)[CH]1.[CH]1[CH][CH]C(P(c2ccccc2)c2ccccc2)[CH]1.[Cl][Pd][Cl].[Fe].[Na+].[Na+]>O=S(=O)(c1ccc(Cl)cc1)N1CCN(c2ccc(-c3ccc4cc[nH]c4c3)cn2)CC1

Participants

8

Reactant 2

HCID 6764936-BromoindoleHCID 179989081-(4-Chlorobenzene-1-sulfonyl)-4-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]piperazine

Product 1

HCID 178527351HCID 178527351, compoundYield 72%

Reagents, catalysts & solvents 5

HCID 10340Sodium CarbonateReagentHCID 178477754HCID 178477754, compoundCatalystHCID 962WaterSolventHCID 80711,2-DimethoxyethaneSolvent2×HCID 741954,4'-Bis(1,1-dimethylethyl)-1,1'-biphenylInternal standard

Conditions

Temperature
85 °C

Workup

  1. stirringNo procedure recorded

Sources & evidence

ORD record
ord-59a90ec0f3554a60aa55efcee046d730
Source dataset
Pd_CN_Coupling_Informer_Library
Original link
View source

Reaction notes

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