Thionyl Chloride → HCID 13336346, compound

HRID 1788720Notes

Reaction equation

HRID 1788720 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:17]=[C:16]([C:18](O)=[O:19])[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[N:9]=1.S(Cl)(Cl)=O.[CH3:25][NH:26][CH:27]([CH2:29][CH3:30])[CH3:28]>>[CH3:25][N:26]([CH:27]([CH3:28])[CH2:29][CH3:30])[C:18]([C:16]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[N:9]=[C:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[Cl:1])[CH:17]=1)=[O:19]

Participants

4

Reactant 3

HCID 24386Thionyl ChlorideHCID 111026N-Methyl-2-butanamineHCID 2691712-(2-chlorophenyl)quinoline-4-carboxylic acid

Product 1

HCID 13336346HCID 13336346, compound

Procedure

The procedure of Example 3 is followed using 2-(2-chlorophenyl)-quinoline-4-carboxylic acid (5.7 g), thionyl chloride (15 ml) and N-methylbut-2-ylamine (15 ml) as the starting materials.

Sources & evidence

ORD record
ord-620b6e9defaf429f96f6b5bd0103afc4
Source dataset
uspto-grants-1987_08
Patent number
US04684652

Reaction notes

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