Iodoethane → 2,7-Diethyl-4-oxo-4,7-dihydrothieno[2,3-b]pyridine-5-carboxylic acid

HRID 1679120Notes

Reaction equation

[CH2:1]([C:3]1[S:17][C:6]2=[N:7][CH:8]=[C:9]([C:12]([O:14]CC)=[O:13])[C:10]([OH:11])=[C:5]2[CH:4]=1)[CH3:2].[CH2:18](I)[CH3:19]>>[CH2:1]([C:3]1[S:17][C:6]2[N:7]([CH2:18][CH3:19])[CH:8]=[C:9]([C:12]([OH:14])=[O:13])[C:10](=[O:11])[C:5]=2[CH:4]=1)[CH3:2]

Participants

Reactant 2

HCID 6340Iodoethane

HCID 178469716HCID 178469716, compound

Product 1

HCID 203637232,7-Diethyl-4-oxo-4,7-dihydrothieno[2,3-b]pyridine-5-carboxylic acid

Procedure

In a manner similar to that described in Example 13, ethyl 2-ethyl-4-hydroxythieno(2,3-b)pyridine-5-carboxylate is reacted with ethyl iodine to obtain 2,7-diethyl-4,7-dihydro-4-oxothieno-(2,3-b)pyridine-5-carboxylic acid. Recrystallization from methanol gives colorless prisms melting at 197°-198° C.

Sources & evidence

ORD record: ord-8433770c828b4e2194128818d6063ca7
Source dataset: uspto-grants-1978_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04079060

Reaction notes

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