Triethylamine → Quinoline-4-carboxylic acid (alpha-methyl-delta-diethylaminobutyl)amide

HRID 1395048Notes

Reaction equation

HRID 1395048 reaction equation
[CH2:1]([N:3]([CH2:6][CH2:7][CH2:8][CH:9]([NH2:11])[CH3:10])[CH2:4][CH3:5])[CH3:2].Cl.[N:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[C:16]([C:23](Cl)=[O:24])=[CH:15][CH:14]=1.C(N(CC)CC)C>O>[CH3:10][CH:9]([NH:11][C:23]([C:16]1[C:17]2[C:22](=[CH:21][CH:20]=[CH:19][CH:18]=2)[N:13]=[CH:14][CH:15]=1)=[O:24])[CH2:8][CH2:7][CH2:6][N:3]([CH2:4][CH3:5])[CH2:1][CH3:2]

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 78953NovoldiamineHCID 12373997Quinoline-4-carbonyl chloride hydrochloride

Product 1

HCID 86736974Quinoline-4-carboxylic acid (alpha-methyl-delta-diethylaminobutyl)amide

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

2-[2'-(5"-nitrofuryl-2")vinyl]quinoline-4-carboxylic acid (α-methyl-δ-diethylaminobutyl)amide was prepared from 1.58 g (0.01 mol.) of diethylamino-4-aminopentane and 3.65 g (0.01 mol.) of 2-[2'-(5"-nitrofuryl-2")vinyl]quinoline-4-carboxylic acid chloride hydrochloride in 50 ml of water in the presence of triethylamine. The process was conducted as described in Example 5.

Sources & evidence

ORD record
ord-b775b91c71bb4b2597ae21fb2ec7a4ff
Source dataset
uspto-grants-1980_05
Patent number
US04201784

Reaction notes

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