Sodium Hydroxide → HCID 67756616, compound

HRID 1195759Notes

Reaction equation

HRID 1195759 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[Al+3].[Cl-].[Cl-].[CH3:11][N:12]1[C:18]2=[C:19]3[C:24](=[N:25][C:26]4[CH2:27][CH2:28][CH2:29][CH:16]([C:17]=42)[S:15][CH2:14][C:13]1=O)[CH:23]=[CH:22][CH:21]=[CH:20]3.[OH-].[Na+].[C:33]([OH:40])(=[O:39])/[CH:34]=[CH:35]\[C:36]([OH:38])=[O:37]>O1CCCC1>[C:33]([OH:40])(=[O:39])/[CH:34]=[CH:35]\[C:36]([OH:38])=[O:37].[CH3:11][N:12]1[C:18]2=[C:19]3[C:24](=[N:25][C:26]4[CH2:27][CH2:28][CH2:29][CH:16]([C:17]=42)[S:15][CH2:14][CH2:13]1)[CH:23]=[CH:22][CH:21]=[CH:20]3

Participants

7

Procedure

To 1M lithium aluminum hydride in tetrahydrofuran (14.1 ml), diluted with tetrahydrofuran (50 ml) was added aluminum chloride (1.9 g), followed by 1,3,4a,5,6,7-hexahydro-1-methyl-2H-quino-[4,3,2-ef][1,4]benzthiazepin-2-one (3.42 g). After stirring for 1 hr, the reaction mixture was poured into iced sodium hydroxide solution and extracted three times with ethyl acetate. The combined organic extracts were washed with water, saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was dissolved in methanol and treated with maleic acid (1.1 eq). Crystallization with ethyl ether followed by recrystallization from methanol/ethyl ether gave 3.17 g (73.0%) of product, mp 200°-201° C. (dec).

Workup

  1. extractionextracted three times with ethyl acetate
  2. washThe combined organic extracts were washed with water, saturated sodium chloride solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. dissolutionThe residue was dissolved in methanol
  7. customCrystallization with ethyl ether
  8. customfollowed by recrystallization from methanol/ethyl ether

Sources & evidence

ORD record
ord-d4e4aa88f8ec489b8ab038b57e7d1cda
Source dataset
uspto-grants-1992_05
Patent number
US05112829

Reaction notes

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