HCID 178431747, compound → HCID 178431108, compound

HRID 1491103Notes

Reaction equation

HRID 1491103 reaction equation
CC1(C(=O)Nc2c(F)c(F)c(C(F)(F)F)c(F)c2F)CCCCCC1>CC#N.CC(=O)O.CC(=O)O.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.CC[N+](CC)(CC)CC.COc1cc(OC)c2ccccc2n1.F[B-](F)(F)F.O=C(O)O.[K].[Pd]>CC1(C)OB(CC2(C(=O)Nc3c(F)c(F)c(C(F)(F)F)c(F)c3F)CCCCCC2)OC1(C)C

Participants

9

Reactant 1

HCID 178431747HCID 178431747, compound

Product 1

HCID 178431108HCID 178431108, compoundYield 68%

Reagents, catalysts & solvents 7

HCID 176Acetic AcidReagentHCID 1424362,4-DimethoxyquinolineReagentHCID 2724277Tetraethylammonium tetrafluoroborateReagentHCID 2733548Bis(pinacolato)diboraneReagentHCID 45051578carbonic acid, potassium saltReagentHCID 58759193palladium(I) acetateCatalystHCID 6342AcetonitrileSolvent

Conditions

Temperature
80 °C

Sources & evidence

ORD record
ord-2323bb448acf49169b8a4e9b899b8da0
Source dataset
Borylation dataset from Roche

Reaction notes

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