Tolmetin → HCID 131730794, compound

HRID 1888341Notes

Reaction equation

HRID 1888341 reaction equation
C(OC(C)C)(C)C.[CH3:8][NH:9][CH2:10][CH2:11][C@H:12]([O:18][C:19]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH:22]=[CH:21][CH:20]=1)[C:13]1[S:17][CH:16]=[CH:15][CH:14]=1.[CH3:29][C:30]1[CH:31]=[CH:32][C:33]([C:36]([C:38]2[N:42]([CH3:43])[C:41]([CH2:44][C:45]([OH:47])=[O:46])=[CH:40][CH:39]=2)=[O:37])=[CH:34][CH:35]=1>C(OCC)(=O)C>[CH3:8][NH:9][CH2:10][CH2:11][C@H:12]([O:18][C:19]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH:22]=[CH:21][CH:20]=1)[C:13]1[S:17][CH:16]=[CH:15][CH:14]=1.[CH3:29][C:30]1[CH:31]=[CH:32][C:33]([C:36]([C:38]2[N:42]([CH3:43])[C:41]([CH2:44][C:45]([OH:47])=[O:46])=[CH:40][CH:39]=2)=[O:37])=[CH:34][CH:35]=1

Participants

5

Procedure

Diisopropyl ether was added drop wise to a solution of (S)-duloxetine (289 mg, 0.97 mmol) and tolmetin (500 mg, 1.94 mmol, 2 eq) in ethyl acetate (1 mL) at reflux until precipitation started. Following, the minimum amount of ethyl acetate was added drop wise to reach complete dissolution again. The solution was then cooled to room temperature, and slowly stirred during 48 h. The resulting suspension was filtered off, washed with cold ethyl acetate and dried under vacuum (10 mm Hg) at 40° C. for 4 hours to give a solid corresponding to a 1:2 ratio (S)-duloxetine-tolmetin co-crystal (700 mg, 89% yield).

Workup

  1. temperatureat reflux until precipitation
  2. dissolutiondissolution again
  3. filtrationThe resulting suspension was filtered off
  4. washwashed with cold ethyl acetate
  5. customdried under vacuum (10 mm Hg) at 40° C. for 4 hours

Sources & evidence

ORD record
ord-6f26a955ebbe48e18968a3407a3eb61d
Source dataset
uspto-grants-2013_08
Patent number
US08501802B2

Reaction notes

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