Trifluoroacetic acid → HCID 59835824, compound
Reaction equation
FC(F)(F)C(O)=O.[Cl:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:16]=[CH:17][C:18]([C:21]#[C:22][C:23]3[CH:46]=[CH:45][C:26]([O:27][CH2:28][CH2:29][N:30]([CH3:44])[CH:31]4[CH2:36][CH2:35][N:34](C(OC(C)(C)C)=O)[CH2:33][CH2:32]4)=[CH:25][CH:24]=3)=[N:19][CH:20]=2)=[CH:11][CH:10]=1>C(Cl)Cl>[Cl:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:16]=[CH:17][C:18]([C:21]#[C:22][C:23]3[CH:24]=[CH:25][C:26]([O:27][CH2:28][CH2:29][N:30]([CH3:44])[CH:31]4[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]4)=[CH:45][CH:46]=3)=[N:19][CH:20]=2)=[CH:11][CH:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
60 μL (0.8 mmol) trifluoroacetic acid are added to a solution of 22 mg (0.04 mmol) tert-butyl 4-[(2-{4-[5-(4-chloro-phenyl)-pyridin-2-ylethynyl]-phenoxy}-ethyl)-methyl-amino]-piperidin-1-carboxylate in 5 mL DCM and the reaction mixture is stirred for 24 h at RT. The mixture is evaporated down i. vac. and the residue is stirred with diethyl ether. The precipitate is suction filtered, washed with diethyl ether and dried.
Workup
- customThe mixture is evaporated down i
- stirringand the residue is stirred with diethyl ether
- filtrationfiltered
- washwashed with diethyl ether
- customdried
Sources & evidence
- ORD record
- ord-8d34fc7537944a3f9c9b37c5eae98772
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618132B2
Reaction notes
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