Trifluoroacetic acid → HCID 11377163, compound
Reaction equation
[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].C(OC([CH:15]1[NH:20][CH2:19][C:18]2[S:21][C:22]([C:24]([N:26]3[CH2:31][CH2:30][N:29]([S:32]([C:35]4[CH:44]=[CH:43][C:42]5[C:37](=[CH:38][CH:39]=[C:40]([Cl:45])[CH:41]=5)[CH:36]=4)(=[O:34])=[O:33])[CH2:28][CH:27]3[C:46](=[O:48])[NH2:47])=[O:25])=[N:23][C:17]=2[CH2:16]1)=O)(C)(C)C>ClCCl>[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[C:46]([CH:27]1[CH2:28][N:29]([S:32]([C:35]2[CH:44]=[CH:43][C:42]3[C:37](=[CH:38][CH:39]=[C:40]([Cl:45])[CH:41]=3)[CH:36]=2)(=[O:34])=[O:33])[CH2:30][CH2:31][N:26]1[C:24]([C:22]1[S:21][C:18]2[CH2:19][NH:20][CH2:15][CH2:16][C:17]=2[N:23]=1)=[O:25])(=[O:48])[NH2:47]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To trifluoroacetic acid (1 ml), a solution of 1-[(6-tert-butoxycarbonyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]-2-carbamoyl-4-[(6-chloronaphthalen-2-yl)sulfonyl]piperazine (303 mg) dissolved in dichloromethane (1 ml) was added, followed by concentration under reduced pressure. The resulting precipitate was collected by filtration and washed with diethyl ether, whereby the title compound (263 mg, 83%) was obtained.
Workup
- additionwas added
- concentrationfollowed by concentration under reduced pressure
- filtrationThe resulting precipitate was collected by filtration
- washwashed with diethyl ether, whereby the title compound (263 mg, 83%)
- customwas obtained
Sources & evidence
- ORD record
- ord-0f5374da0df14489bb0ce4e7ffeff857
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06525042B1
Reaction notes
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