HCID 21558236, compound → HCID 178449638, compound

HRID 1491237Notes

Reaction equation

HRID 1491237 reaction equation
CC(C)(C)NC(=O)Oc1cccc(Cl)c1>C1=CCCC=CCC1.C1=CCCC=CCC1.CC(C)(C)c1ccnc(-c2cc(C(C)(C)C)ccn2)c1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.CC1(C)OBOC1(C)C.COC(C)(C)C.C[OH2+].C[OH2+].[Ir].[Ir]>CC(C)(C)NC(=O)Oc1cc(Cl)cc(B2OC(C)(C)C(C)(C)O2)c1

Participants

7

Reactant 1

HCID 21558236HCID 21558236, compound

Product 1

HCID 178449638HCID 178449638, compoundYield 50%

Reagents, catalysts & solvents 5

HCID 2733548Bis(pinacolato)diboraneReagentHCID 27347684,4,5,5-Tetramethyl[1,3,2]dioxaborolaneReagentHCID 42491874,4'-Di-tert-butyl-2,2'-bipyridylReagentHCID 76001521Bis(1,5-cyclooctadiene)dimethoxydiiridiumCatalystHCID 15413tert-Butyl methyl etherSolvent

Conditions

Temperature
50 °C

Sources & evidence

ORD record
ord-e8b13c5aed8e473282aaeb342d6dc961
Source dataset
Borylation dataset from Roche

Reaction notes

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