(2-Methoxypyridin-4-yl)boronic acid → HCID 57389310, compound

HRID 1184759Notes

Reaction equation

HRID 1184759 reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([CH:14]2[O:23][C:17]3=[CH:18][N:19]=[C:20](Cl)[CH:21]=[C:16]3[CH2:15]2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:24][O:25][C:26]1[CH:31]=[C:30](B(O)O)[CH:29]=[CH:28][N:27]=1>>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([CH:14]2[O:23][C:17]3=[CH:18][N:19]=[C:20]([C:30]4[CH:29]=[CH:28][N:27]=[C:26]([O:25][CH3:24])[CH:31]=4)[CH:21]=[C:16]3[CH2:15]2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 23546919(2-Methoxypyridin-4-yl)boronic acidHCID 866748954-(5-Chloro-2,3-dihydrofuro[2,3-c]pyridin-2-yl)piperidine-1-carboxylic acid tert-butyl ester

Product 1

HCID 57389310HCID 57389310, compound

Procedure

The title compound is prepared from 4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester and 2-methoxypyridine-4-boronic acid following a procedure analogous to that described in Example 28. LC (method 10): tR=1.76 min; Mass spectrum (ESI+): m/z=412 [M+H]+.

Sources & evidence

ORD record
ord-83606ef10bc949b4a943f106743d5f52
Source dataset
uspto-grants-2014_03
Patent number
US08669271B2

Reaction notes

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