HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892627Generated: October 31, 2026
Hydrochloric Acid → HCID 19090376, compound
https://huagongshe.com/reaction/892627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15069584 | HCID 15069584 | — |
| Catalyst | Dichlorocobalt hexahydrate | HCID 517166 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19090376 | HCID 19090376 | 20.1% |
Reaction Steps
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 chromatogarphy on silica gel, and neutralized with hydrogen chloride to give the title compound (yield 20.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05118806 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-2511238144ed4530939f763bb47fe2c9 |
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| Source note | uspto-grants-1992_06 |
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