HCID 53986269, compound → HCID 178424121, compound

HRID 1491497Notes

Reaction equation

HRID 1491497 reaction equation
Cc1ccccc1C=NN(C)C>C(=NN(Cc1ccccc1)Cc1ccccc1)c1ccccn1.C1=CCCC=CCC1.C1=CCCC=CCC1.C1CCOC1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.CC1(C)OBOC1(C)C.C[OH2+].C[OH2+].[Ir].[Ir]>Cc1cccc(B2OC(C)(C)C(C)(C)O2)c1C=NN(C)C

Participants

7

Reactant 1

HCID 53986269HCID 53986269, compound

Product 1

HCID 178424121HCID 178424121, compoundYield 88%

Reagents, catalysts & solvents 5

HCID 2733548Bis(pinacolato)diboraneReagentHCID 27347684,4,5,5-Tetramethyl[1,3,2]dioxaborolaneReagentHCID 67601456N,N-Dibenzyl-N'-(pyridin-2-ylmethylene)hydrazineReagentHCID 76001521Bis(1,5-cyclooctadiene)dimethoxydiiridiumCatalystHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
80 °C

Procedure

Following the general procedure, column chromatography in neutral alumina (EtOAc/n-hexane 1:10) afforded 11b (127 mg, 88 %) as a yellow oil.

Sources & evidence

ORD record
ord-895c802f0ca6427386e5a180b5798e76
Source dataset
Borylation dataset from Roche

Reaction notes

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