Trifluoroacetic acid → HCID 86687442, compound
Reaction equation
[F:1][C:2]1[C:33]([F:34])=[C:32]([F:35])[C:31]([F:36])=[C:30]([F:37])[C:3]=1[O:4][S:5]([C:8]1[CH:9]=[C:10]2[C:15](=[CH:16][CH:17]=1)[C:14]([CH:18]1[CH2:22][CH2:21][CH2:20][N:19]1C(OC(C)(C)C)=O)=[N:13][CH:12]=[CH:11]2)(=[O:7])=[O:6].[C:38]([OH:44])([C:40]([F:43])([F:42])[F:41])=[O:39]>C(Cl)Cl>[F:41][C:40]([F:43])([F:42])[C:38]([OH:44])=[O:39].[NH:19]1[CH2:20][CH2:21][CH2:22][CH:18]1[C:14]1[C:15]2[C:10](=[CH:9][C:8]([S:5]([O:4][C:3]3[C:2]([F:1])=[C:33]([F:34])[C:32]([F:35])=[C:31]([F:36])[C:30]=3[F:37])(=[O:6])=[O:7])=[CH:17][CH:16]=2)[CH:11]=[CH:12][N:13]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A round-bottom flask was charged with tert-butyl 2-(6-((perfluorophenoxy)sulfonyl)isoquinolin-1-yl)pyrrolidine-1-carboxylate (1.02 g, 1.873 mmol) and DCM (5.0 mL) to give a light yellow solution. TFA (1.443 ml, 18.73 mmol) was added in one portion to give a yellow solution. The reaction was stirred for two hours. The reaction was concentrated, dissolved in diethyl ether, and sonicated until a fine white solid triturated out of solution. The solids were filtered, washed with diethyl ether, and vacuum dried overnight to afford perfluorophenyl 1-(pyrrolidin-2-yl)isoquinoline-6-sulfonate 2,2,2-trifluoroacetate as a white solid. (ESI) 445.3 (M+H)+.
Workup
- customto give a light yellow solution
- customto give a yellow solution
- concentrationThe reaction was concentrated
- dissolutiondissolved in diethyl ether
- customsonicated until a fine white solid
- customtriturated out of solution
- filtrationThe solids were filtered
- washwashed with diethyl ether, and vacuum
- customdried overnight
Sources & evidence
- ORD record
- ord-ca87ff97879d4182b906165bc0b79560
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09012443B2
Reaction notes
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