Methyl 2,6-dichloropyridine-3-carboxylate → 3-Hydroxy-6-chlorofuro[2,3-b]pyridine-2-carboxylic acid ethyl ester

HRID 1508235Notes

Reaction equation

HRID 1508235 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[O:14][C:9]2[N:10]=N[CH:12]=[CH:13][C:8]=2[C:7]=1[OH:15])=[O:5])[CH3:2].COC(=O)C1C=C[C:22]([Cl:25])=NC=1Cl>>[CH2:1]([O:3][C:4]([C:6]1[O:14][C:9]2=[N:10][C:22]([Cl:25])=[CH:12][CH:13]=[C:8]2[C:7]=1[OH:15])=[O:5])[CH3:2]

Participants

3

Procedure

This compound was prepared using a method analogous to that of 5-hydroxyfuro[2,3-c]pyridazine-6-carboxylic acid ethyl ester (A.2.3.1), 2,6-dichloronicotinic acid methyl ester replacing 3-chloropyridazine-4-carboxylic acid ethyl ester;

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-397777b148e846758fcb874807565779
Source dataset
uspto-grants-2015_12
Patent number
US09221832B2

Reaction notes

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