Methyl iodide → HCID 18929787, compound

HRID 1598580Notes

Reaction equation

[CH2:1]([S:4]([NH:7][CH:8]1[CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[C:13]([C:17]3[CH:18]=[CH:19][C:20](=[O:23])[NH:21][N:22]=3)[CH:14]=2)[CH2:9]1)(=[O:6])=[O:5])[CH2:2][CH3:3].[CH3:24]I>>[CH2:1]([S:4]([NH:7][CH:8]1[CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[C:13]([C:17]3[CH:18]=[CH:19][C:20](=[O:23])[N:21]([CH3:24])[N:22]=3)[CH:14]=2)[CH2:9]1)(=[O:6])=[O:5])[CH2:2][CH3:3]

Participants

Reactant 2

HCID 6328Methyl iodide

HCID 18929754HCID 18929754, compound

Product 1

HCID 18929787HCID 18929787, compound

Procedure

2-n-Propylsulfonylamino-5-[pyridazin-3(2H)-on-6-yl]indane and methyl iodide were reacted in the same manner as in Example 91 to obtain 2-n-propylsulfonylamino-5-[2-methylpyridazin-3(2H)-on-6-yl]indane.

Sources & evidence

ORD record: ord-cb07413b7fcf4710a898d7c5ccd66570
Source dataset: uspto-grants-1998_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05739132

Reaction notes

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