HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285439Generated: October 29, 2026
Hydrochloric Acid → 6-(1-Hydroxy-2-piperazinylbutyl)-3,4-dihydrocarbostyril
https://huagongshe.com/reaction/1285439
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-(1-Oxo-2-piperazinylbutyl)-3,4-dihydrocarbostyril | HCID 57294315 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(1-Hydroxy-2-piperazinylbutyl)-3,4-dihydrocarbostyril | HCID 57078195 | — |
Reaction Steps
2.5 Grams of 6-(1-oxo-2-piperazinylbutyl)-3,4-dihydrocarbostyril was mixed in 80 ml of methanol and 1.6 g of sodium borohydride was added gradually under stirring at a room temperature in 15 minutes and further stirred at a room temperature for 2 hours. To the reaction mixture was added 5 ml of concentrated hydrochloric acid and the reaction mixture was concentrated under a reduced pressure to dryness. The residue thus obtained was dissolved by adding 10 ml of water and the pH of the solution was adjusted to 6-7 by adding 2N-sodium hydroxide aqueous solution at a room temperature and stirred to precipitate crystals. The crystals were collected by filtration washed with water and dried to obtain 1.2 g of 6-(1-hydroxy-2-piperazinylbutyl)-3,4-dihydrocarbostyril in colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04567187 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-14b73d585d864afdb54c2ad12133770b |
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| Source note | uspto-grants-1986_01 |
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