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4-Bromo-2-methylpyridine → tert-Butyl 2-(2-methylpyridin-4-yl)pyrrolidine-1-carboxylate

HRID 2031406
Notes
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Reaction equation

HRID 2031406 reaction equation
[CH3:1][c:2]1[n:7][cH:6][cH:5][c:4](Br)[cH:3]1.[K+].[CH3:8][C:9]([O:12][C:13]([N:15]1[CH:19]([B-](F)(F)F)[CH2:18][CH2:17][CH2:16]1)=[O:14])([CH3:11])[CH3:10]>>[CH3:1][c:2]1[n:7][cH:6][cH:5][c:4]([CH:19]2[N:15]([C:13]([O:12][C:9]([CH3:11])([CH3:10])[CH3:8])=[O:14])[CH2:16][CH2:17][CH2:18]2)[cH:3]1
ParticipantsConditionsSources & evidenceReaction notes

Participants

8

Reactant 2

HCID 27628354-Bromo-2-methylpyridineHCID 74787601Potassium (1-((tert-butoxy)carbonyl)pyrrolidin-2-yl)trifluoroboranuide

Product 1

HCID 102543294tert-Butyl 2-(2-methylpyridin-4-yl)pyrrolidine-1-carboxylate

Reagents, catalysts & solvents 5

HCID 10796Cesium carbonateReagentHCID 204456,6'-Bi-2-picolineCatalystHCID 3032389Bis(1,5-cyclooctadiene) nickelCatalystHCID 6228DimethylformamideSolventHCID 117669-PhenylanthraceneInternal standard

Conditions

Temperature
25 °C

Sources & evidence

ORD record
ord-5a3a3df8f0cd42ef85a43591eb5ecb94
Source dataset
39k HTE dataset from Pfizer
DOI
10.1038/s41557
Original link
View source

Reaction notes

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On this pageParticipantsConditionsSources & evidenceReaction notes