Sodium borohydride → HCID 59662588, compound

HRID 1015082Notes

Reaction equation

Br[C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][N:8]=[CH:9]2)=[CH:4][CH:3]=1.C[Sn](C)(C)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=1.[BH4-].[Na+]>>[N:15]1[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=1[C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][NH:8][CH2:9]2)=[CH:4][CH:3]=1

Participants

Reactant 3

HCID 4311764Sodium borohydride

HCID 11021057Pyridine, 2-(trimethylstannyl)-

HCID 122574417-Bromoisoquinoline

Product 1

HCID 59662588HCID 59662588, compound

Procedure

In close analogy to the procedure described above, 7-Bromo-isoquinoline is reacted with 2-trimethylstannyl-pyridine and sodium borohydride to provide the title compound.

Sources & evidence

ORD record: ord-43edaaa15c6a44f0a9c7a18d71104b32
Source dataset: uspto-grants-2011_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07985753B2

Reaction notes

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