HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

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

HRID 2031400
Notes
Print preview

Reaction equation

HRID 2031400 reaction equation
[K+].[CH3:1][C:2]([O:5][C:6]([N:8]1[CH:12]([B-](F)(F)F)[CH2:11][CH2:10][CH2:9]1)=[O:7])([CH3:4])[CH3:3].[CH3:13][c:14]1[n:19][cH:18][cH:17][c:16](Br)[cH:15]1>>[CH3:13][c:14]1[n:19][cH:18][cH:17][c:16]([CH:12]2[N:8]([C:6]([O:5][C:2]([CH3:4])([CH3:3])[CH3:1])=[O:7])[CH2:9][CH2:10][CH2:11]2)[cH:15]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 241032-(Pyridin-2-yl)quinoline-4-carboxylic acidCatalystHCID 3032389Bis(1,5-cyclooctadiene) nickelCatalystHCID 6228DimethylformamideSolventHCID 117669-PhenylanthraceneInternal standard

Conditions

Temperature
25 °C

Sources & evidence

ORD record
ord-ab0e1a055771489d9d82c3305d30a89f
Source dataset
39k HTE dataset from Pfizer
DOI
10.1038/s41557
Original link
View source

Reaction notes

Loading…

On this pageParticipantsConditionsSources & evidenceReaction notes