Hydrochloric Acid → HCID 66630488, compound

HRID 2382484Notes

Reaction equation

HRID 2382484 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]=1

Participants

5

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

  1. customThe title compound is prepared
  2. extractionextracting into ethyl acetate
  3. dry with materialThe organic phase is dried over magnesium sulfate
  4. filtrationfiltered
  5. customthe volatile components removed under reduced pressure

Sources & evidence

ORD record
ord-7261aa84873543479b5adf3b6fbc7467
Source dataset
uspto-grants-2012_09
Patent number
US08258141B2

Reaction notes

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