Hydrochloric Acid → HCID 19090376, compound

HRID 1031898Notes

Reaction equation

HRID 1031898 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:10][C:11]3[NH:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]=3[N:18]=2)=[CH:5][C:4]=1[CH3:19])#[N:2].[BH4-].[Na+].[ClH:22]>CO.O1CCCC1.O.O.O.O.O.O.[Co](Cl)Cl>[ClH:22].[ClH:22].[NH2:2][CH2:1][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:10][C:11]3[NH:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]=3[N:18]=2)=[CH:5][C:4]=1[CH3:19]

Participants

7

Procedure

A solution of 2-(4-cyano-3-methylphenyl)-5,6,7,8-tetrahydro-4H-thiazolo[5,4-b]azepine (20 g) and cobalt chloride hexahydrate (35.3 g) in a mixture of methanol (90 ml) and tetrahydrofuran (60 ml) was ice-cooled, followed by addition of a powder of sodium borohydride (33.1 g) gradually, and further stirred for 20 hrs. at room temperature. After acidifying with an aqueous 4N-hydrochloric acid, the reaction mixture was extracted with diethyl ether. The aqueous layer was alkalified with an aqueous ammonia and extracted with chloroform. The extract was dried over anhydrous magnesium sulfate, and distilled under reduced pressure. The residue was purified by a column chromatography on silica gel, and neutralized with hydrogen chloride to give the title compound (yield 20.1%).

Workup

  1. temperaturecooled
  2. customat room temperature
  3. extractionthe reaction mixture was extracted with diethyl ether
  4. extractionextracted with chloroform
  5. dry with materialThe extract was dried over anhydrous magnesium sulfate
  6. distillationdistilled under reduced pressure
  7. customThe residue was purified by a column chromatography on silica gel

Sources & evidence

ORD record
ord-c76059d0035947f08bb25f401bdfddb0
Source dataset
uspto-grants-1990_09
Patent number
US04956360

Reaction notes

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