Methanesulfonyl chloride → HCID 10411609, compound

HRID 1268807Notes

Reaction equation

HRID 1268807 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][N:5]1[C:17]2[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=[C:9]([NH2:18])[C:8]=2[N:7]=[C:6]1[CH2:19][CH2:20][CH2:21][O:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.[CH3:29][S:30](Cl)(=[O:32])=[O:31]>C(Cl)(Cl)Cl>[NH2:18][C:9]1[C:8]2[N:7]=[C:6]([CH2:19][CH2:20][CH2:21][O:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[N:5]([CH2:4][CH2:3][CH2:2][NH:1][S:30]([CH3:29])(=[O:32])=[O:31])[C:17]=2[C:16]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[N:10]=1

Participants

4

Reactant 2

HCID 31297Methanesulfonyl chlorideHCID 22344439HCID 22344439, compound

Product 1

HCID 10411609HCID 10411609, compound

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Procedure

Using the general method of Example 242, except that chloroform was used in place of dichloromethane, 1-(3-aminopropyl)-2-(3-phenoxypropyl)-1H-imidazo[4,5-c]quinolin-4-amine (2.00 g, 5.32 mmol) was reacted with methanesulfonyl chloride (3+ g) to provide 1.38 g of N-{3-[4-amino-2-(3-phenoxypropyl)-1H-imidazo[4,5-c]quinolin-1-yl]propyl}methanesulfonamide as a solid, m.p. 176–178° C. Analysis: Calculated for C23H27N5O3S: % C, 60.91; % H, 6.00; % N, 15.44. Found: % C, 60.71; % H, 5.98; % N, 15.45.

Sources & evidence

ORD record
ord-4c15bf3860c1400dac4c613414a82352
Source dataset
uspto-grants-2007_04
Patent number
US07199131B2

Reaction notes

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