Oleoyl chloride → HCID 67710064, compound

HRID 2257183Notes

Reaction equation

HRID 2257183 reaction equation
[NH2:1][C:2]1[C:11]([S:12][CH3:13])=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2.[C:14](Cl)(=[O:32])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]/[CH:22]=[CH:23]\[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31]>>[CH3:13][S:12][C:11]1[C:2]([NH:1][C:14](=[O:32])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]/[CH:22]=[CH:23]\[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])=[C:3]2[C:8](=[CH:9][CH:10]=1)[N:7]=[CH:6][CH:5]=[CH:4]2

Participants

3

Reactant 2

HCID 5364783Oleoyl chlorideHCID 103976605-Amino-6-methylthioquinoline

Product 1

HCID 67710064HCID 67710064, compound

Procedure

5-Amino-6-methylthioquinoline, prepared as described in Example 34, and commercially available oleoyl chloride were coupled to give the title compound according to the procedure described in Example 25. Mass psectrum m/e: 454.3 (M+).

Sources & evidence

ORD record
ord-35771035cbdc42ee9d4c3dc52109c5a8
Source dataset
uspto-grants-1997_08
Patent number
US05656634

Reaction notes

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