Sulfuric Acid → HCID 178473868, compound
Reaction equation
C(O)(C(F)(F)F)=O.[C:8]([N:11]1[CH2:15][C@H:14]([OH:16])[CH2:13][C@H:12]1[C:17]([NH:19][C@H:20]([C:28]([C:30]1[S:31][C:32]2[CH:38]=[CH:37][CH:36]=[CH:35][C:33]=2[N:34]=1)=[O:29])[CH2:21][CH2:22][CH2:23][NH:24][C:25](=[NH:27])[NH2:26])=[O:18])(=[O:10])[CH3:9].[S:39](=[O:43])(=[O:42])([OH:41])[OH:40]>C(#N)C>[S:39]([OH:43])([OH:42])(=[O:41])=[O:40].[C:8]([N:11]1[CH2:15][C@H:14]([OH:16])[CH2:13][C@H:12]1[C:17]([NH:19][C@H:20]([C:28]([C:30]1[S:31][C:32]2[CH:38]=[CH:37][CH:36]=[CH:35][C:33]=2[N:34]=1)=[O:29])[CH2:21][CH2:22][CH2:23][NH:24][C:25](=[NH:26])[NH2:27])=[O:18])(=[O:10])[CH3:9]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of the TFA salt of the single diastereomer (2S,4R)-1-Acetyl-N-[(1S)-1-(2-benzothiazolylcarbonyl)-4-[[imino(amino)methyl]amino]butyl]-4-hydroxypyrrolidine-2-carboxamide (0.30 g, 0.493 mmol) in acetonitrile (4 mL) was added a solution of sulfuric acid (48.3 mg, 0.493 mmol) in acetonitrile (1 mL). A suspension formed upon mixing. The suspension was heated to partially dissolve the solid, then cooled to precipitate the title compound as a solid. The solid was filtered and dried in a vacuum oven at 30° C.
Workup
- customA suspension formed
- additionupon mixing
- temperatureThe suspension was heated
- dissolutionto partially dissolve the solid
- temperaturecooled
- customto precipitate the title compound as a solid
- filtrationThe solid was filtered
- customdried in a vacuum oven at 30° C.
Sources & evidence
- ORD record
- ord-e8d7a2bebe73418ba05f100b4bb8a970
- Source dataset
- uspto-grants-2007_04
- Patent number
- US07205384B2
Reaction notes
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