1,4-Dioxane hydrochloride → HCID 86684385, compound
Reaction equation
[C:1]([O:4][CH2:5][C:6]1[C:7]([N:37]2[CH2:49][CH2:48][N:40]3[C:41]4[CH2:42][CH2:43][CH2:44][CH2:45][C:46]=4[CH:47]=[C:39]3[C:38]2=[O:50])=[N:8][CH:9]=[CH:10][C:11]=1[C:12]1[CH:13]=[C:14]([NH:20][C:21]2[CH:36]=[C:24]3[CH2:25][N:26](C(OC(C)(C)C)=O)[CH2:27][CH2:28][N:23]3[N:22]=2)[C:15](=[O:19])[N:16]([CH3:18])[CH:17]=1)(=[O:3])[CH3:2].Cl.O1CCOCC1>ClCCl>[C:1]([O:4][CH2:5][C:6]1[C:7]([N:37]2[CH2:49][CH2:48][N:40]3[C:41]4[CH2:42][CH2:43][CH2:44][CH2:45][C:46]=4[CH:47]=[C:39]3[C:38]2=[O:50])=[N:8][CH:9]=[CH:10][C:11]=1[C:12]1[CH:13]=[C:14]([NH:20][C:21]2[CH:36]=[C:24]3[CH2:25][NH:26][CH2:27][CH2:28][N:23]3[N:22]=2)[C:15](=[O:19])[N:16]([CH3:18])[CH:17]=1)(=[O:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 205e (280 mg, 0.41 mmol), 4.0 M HCl/dioxane (4 mL), and dichloromethane (4 mL) was stirred at room temperature for 2 h. It was then concentrated under reduced pressure to afford 205f as a yellow solid (165 mg, 66%), which was used for the next step without further purification. MS-ESI: [M+H]+ 583.3.
Workup
- concentrationIt was then concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-c924afe2fd9c4580bd6d4bd901971ac9
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09238655B2
Reaction notes
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