Hydrochloric Acid → HCID 66630488, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][O:10][C:11]2[N:19]=[C:18]3[C:14]([N:15]=[CH:16][N:17]3[C@H:20]3[C@@H:24]4[O:25]C(C)(C)[O:27][C@@H:23]4[C@@H:22]([NH:30][C:31](=[O:34])[CH2:32][CH3:33])[CH2:21]3)=[C:13]([NH:35][CH2:36][CH:37]([C:44]3[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=3)[C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=3)[N:12]=2)=[CH:4][CH:3]=1.Cl>C1COCC1.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][O:10][C:11]2[N:19]=[C:18]3[C:14]([N:15]=[CH:16][N:17]3[C@@H:20]3[CH2:21][C@H:22]([NH:30][C:31](=[O:34])[CH2:32][CH3:33])[C@@H:23]([OH:27])[C@H:24]3[OH:25])=[C:13]([NH:35][CH2:36][CH:37]([C:44]3[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=3)[C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=3)[N:12]=2)=[CH:6][CH:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The title compound is prepared by dissolving N-{(3aR,4S,6R,6aS)-6-[2-[2-(4-Chloro-phenyl)-ethoxy]-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-yl}-propionamide (Example 235, Step 2) in THF, adding an equal volume of 1.0M hydrochloric acid, and stirring at room temperature for 48 hours, before diluting with water, and extracting into ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and the volatile components removed under reduced pressure, to yield the title compound.
Workup
- customThe title compound is prepared
- extractionextracting into ethyl acetate
- dry with materialThe organic phase is dried over magnesium sulfate
- filtrationfiltered
- customthe volatile components removed under reduced pressure
Sources & evidence
- ORD record
- ord-afaabd967817470d80ecf4910eb6ae96
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318750B2
Reaction notes
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