Trifluoromethanesulfonyl chloride → HCID 59474729, compound

HRID 1966520Notes

Reaction equation

Cl.Cl.[NH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:16]=1[N:15]=[C:14]([CH3:17])[CH:13]=[C:12]2[NH:18][CH2:19][C:20]1[CH:25]=[CH:24][C:23]([Cl:26])=[C:22]([Cl:27])[CH:21]=1.[F:28][C:29]([F:35])([F:34])[S:30](Cl)(=[O:32])=[O:31]>>[Cl:27][C:22]1[CH:21]=[C:20]([CH:25]=[CH:24][C:23]=1[Cl:26])[CH2:19][NH:18][C:12]1[C:11]2[C:16](=[C:7]([O:6][CH2:5][CH2:4][NH:3][S:30]([C:29]([F:35])([F:34])[F:28])(=[O:32])=[O:31])[CH:8]=[CH:9][CH:10]=2)[N:15]=[C:14]([CH3:17])[CH:13]=1

Participants

Reactant 2

HCID 79000Trifluoromethanesulfonyl chloride

HCID 25217580HCID 25217580, compound

Product 1

HCID 59474729HCID 59474729, compound

Procedure

Preparation was made using a similar procedure as described in example 21. Starting materials were [8-(2-aminoethoxy)-2-methylquinolin-4-yl]-(3,4-dichlorobenzyl)-amine dihydrochloride and trifluoromethanesulfonyl chloride.

Workup

customPreparation

Sources & evidence

ORD record: ord-1de8d3c3e5704e34a711cfe51325dc2c
Source dataset: uspto-grants-2013_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08420670B2

Reaction notes

Loading…