Sulfuric Acid → HCID 21888054, compound
Reaction equation
Cl.[Cl:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][NH:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([C:18]1[CH:19]=[C:20]2[C:25]3=[C:26]([CH2:28][C:29](=[O:30])[N:24]3[CH2:23][CH2:22][CH2:21]2)[CH:27]=1)=[O:17].[S:31](=[O:35])(=[O:34])([OH:33])[OH:32]>>[S:31]([OH:35])([OH:34])(=[O:33])=[O:32].[Cl:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][NH:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([C:18]1[CH:19]=[C:20]2[C:25]3=[C:26]([CH2:28][C:29](=[O:30])[N:24]3[CH2:23][CH2:22][CH2:21]2)[CH:27]=1)=[O:17]Participants
3
Procedure
Using 8-(5-{[2-(2-chlorophenyl)ethyl]amino}pentanoyl)-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-one hydrochloride (205 mg, 0.5 mmol) obtained in Example 39 and sulfuric acid (49 mg, 0.5 mmol) according to the same method as that of Example 360, the title compound was obtained as colorless crystals (218 mg) having a melting point of 155 to 156° C. (dec). elementary analysis as C24H27ClN2O2.H2SO4 calculation value: C, 56.63; H, 5.74; N, 5.50. experimental value: C, 56.42; H, 5.86; N, 5.23.
Sources & evidence
- ORD record
- ord-31920b1ceb33477cbd033d15644f56b6
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07138533B2
Reaction notes
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