1-Iodopropane → HCID 59694439, compound

HRID 899450Notes

Reaction equation

[CH3:1][CH:2]1[CH2:4][CH:3]1/[CH:5]=[CH:6]\[C:7]1[CH:8]=[C:9]([CH:13]=[C:14]([N:16]([CH3:21])[S:17]([CH3:20])(=[O:19])=[O:18])[CH:15]=1)[C:10]([OH:12])=[O:11].[CH2:22](I)[CH2:23]C>>[CH3:1][CH:2]1[CH2:4][CH:3]1/[CH:5]=[CH:6]\[C:7]1[CH:8]=[C:9]([CH:13]=[C:14]([N:16]([CH2:21][CH2:22][CH3:23])[S:17]([CH3:20])(=[O:19])=[O:18])[CH:15]=1)[C:10]([OH:12])=[O:11]

Participants

Reactant 2

HCID 336431-Iodopropane

HCID 59694436HCID 59694436, compound

Product 1

HCID 59694439HCID 59694439, compound

Procedure

This compound was prepared analogously to 3-[(Z)-2-(2-methylcyclopropyl)vinyl]-5-[methyl(methylsulfonyl)amino]benzoic acid, the only difference being the substitution of methyl iodide with propyl iodide in Step D.

Sources & evidence

ORD record: ord-cee0f72095264d0e84fba7be68c93010
Source dataset: uspto-grants-2008_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07354942B2

Reaction notes

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