Hydrochloric Acid → HCID 57737264, compound
Reaction equation
[CH2:1]([O:3][C:4]([N:6]1[C:10]2[S:11][C:12]([C:14]([O:16]C(C)(C)C)=[O:15])=[CH:13][C:9]=2[C:8]([NH:21][C:22](=[O:37])[C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[NH:29][C:30]([C:32]2[NH:33][CH:34]=[CH:35][CH:36]=2)=[O:31])=[N:7]1)=[O:5])[CH3:2].Cl>O1CCOCC1>[CH2:1]([O:3][C:4]([N:6]1[C:10]2[S:11][C:12]([C:14]([OH:16])=[O:15])=[CH:13][C:9]=2[C:8]([NH:21][C:22](=[O:37])[C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[NH:29][C:30]([C:32]2[NH:33][CH:34]=[CH:35][CH:36]=2)=[O:31])=[N:7]1)=[O:5])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The solution of 3-{2-[(1H-Pyrrole-2-carbonyl)-amino]-benzoylamino}-thieno[2,3-c]pyrazole-1,5-dicarboxylic acid 5-tert-butyl ester 1-ethyl ester (460.8 mg, 0.88 mmol) in dioxane (10 mL) was treated with HCl 4M in dioxane (10 mL) overnight, the solvent was then removed and the residue was triturated with diethylether (Et2O, 15 mL) yielding 397 mg (96%) of the product, LC-MS: Rt 3.7; [M+H]+ 468;
Workup
- customthe solvent was then removed
- customthe residue was triturated with diethylether (Et2O, 15 mL)
Sources & evidence
- ORD record
- ord-2a3fcdb7337a4928bf9460a8a63d170c
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07943654B2
Reaction notes
Loading…