Hydrochloric Acid → HCID 66995286, compound
Reaction equation
CCOCC.Cl.[Cl:7][C:8]1[CH:18]=[C:17]([C:19]2[N:24]=[C:23]3[N:25]([CH2:28][C:29]4[CH:30]=[C:31]5[C:36](=[CH:37][CH:38]=4)[N:35]=[CH:34][CH:33]=[CH:32]5)[N:26]=[N:27][C:22]3=[CH:21][CH:20]=2)[CH:16]=[CH:15][C:9]=1[C:10]([NH:12][CH2:13][CH3:14])=[O:11]>C1COCC1>[ClH:7].[Cl:7][C:8]1[CH:18]=[C:17]([C:19]2[N:24]=[C:23]3[N:25]([CH2:28][C:29]4[CH:30]=[C:31]5[C:36](=[CH:37][CH:38]=4)[N:35]=[CH:34][CH:33]=[CH:32]5)[N:26]=[N:27][C:22]3=[CH:21][CH:20]=2)[CH:16]=[CH:15][C:9]=1[C:10]([NH:12][CH2:13][CH3:14])=[O:11]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Ether saturated with HCl (1 ml) was added at 0° C. to a solution of example 119 (0.020 g. 0.045 mmol) in THF (1 ml), and stirred for 15 min. The precipitate formed was filtered, washed with ether and dried under vacuum to afford the title compound as an off-white solid (0.012 g, 56%). M.P.: 151-153° C.
Workup
- customThe precipitate formed
- filtrationwas filtered
- washwashed with ether
- customdried under vacuum
Sources & evidence
- ORD record
- ord-41bfec3762c04469849c92c49d9a7a74
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08481739B2
Reaction notes
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