Trifluoroacetic acid → HCID 86638311, compound
Reaction equation
FC(F)(F)C(O)=O.[CH2:8]([N:19]([CH2:31][C:32]([OH:34])=[O:33])[CH2:20][CH2:21][N:22]([CH2:27][C:28]([OH:30])=[O:29])[CH2:23][C:24]([OH:26])=[O:25])[CH2:9][N:10]([CH2:15][C:16]([OH:18])=[O:17])[CH2:11][C:12]([OH:14])=[O:13].C(OC([NH:42][CH2:43][CH:44]1[CH2:49][CH2:48][CH:47]([CH2:50][NH-:51])[CH2:46][CH2:45]1)=O)(C)(C)C>C(OCC)C>[CH2:20]([N:19]([CH2:31][C:32]([OH:34])=[O:33])[CH2:8][CH2:9][N:10]([CH2:11][C:12]([OH:14])=[O:13])[CH2:15][C:16]([OH:18])=[O:17])[CH2:21][N:22]([CH2:27][C:28]([OH:30])=[O:29])[CH2:23][C:24]([OH:26])=[O:25].[NH2:42][CH2:43][CH:44]1[CH2:49][CH2:48][CH:47]([CH2:50][NH-:51])[CH2:46][CH2:45]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Subsequently, 95 ml of trifluoroacetic acid (produced by Wako Pure Chemical Industries, Ltd.) was added to 9.22 g of the DTPA-mono-(4-(N-tert-butoxycarbonylaminomethyl)cyclohexyl)methylamide obtained above, and, after stirring the mixture for 3 hours, the reaction mixture was added dropwise to diethyl ether to precipitate the reaction product. The reaction product precipitated was collected by suction filtration, and was dried under a reduced pressure, to obtain 11.0 g of DTPA-mono-(4-(aminomethyl)cyclohexyl)methylamide as the objective compound.
Workup
- customobtained above, and,
- customto precipitate the reaction product
- customThe reaction product precipitated
- filtrationwas collected by suction filtration
- customwas dried under a reduced pressure
Sources & evidence
- ORD record
- ord-fb956fc8bcd5488da9fb4f0d9f787de5
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618032B2
Reaction notes
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