HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33231Generated: October 29, 2026
Sodium triacetoxyborohydride → HCID 69311958, compound
https://huagongshe.com/reaction/33231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 69181179 | HCID 69181179 | — |
| Reactant | 4-(4-Methyl-5-quinolin-6-yl-4H-[1,2,4]triazol-3-ylsulfanyl)-butyraldehyde | HCID 86594173 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69311958 | HCID 69311958 | 21% |
Reaction Steps
4-(4-Methyl-5-quinolin-6-yl-4H-[1,2,4]triazol-3-ylsulfanyl)-butyraldehyde (0.1 g, 0.32 mmol) and 7-Ethanesulfonyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine (0.11 g, 0.45 mmol) were stirred at room temperature in dichloromethane (4 ml) for 20 min. Sodium triacetoxyborohydride (71 mg, 0.34 mmol) was then added and the mixture stirred overnight. The mixture was diluted with dichloromethane (50 ml) and washed with saturated sodium bicarbonate solution (30 ml). The aqueous was extracted with further dichloromethane (50 ml) and the combined organic portions were dried (Na2SO4), filtered and evaporated to give a yellow oil. Purification by silica gel chromatography (eluent 10% MeOH:EtOAc) which gave the title compound as a colourless oil (35 mg, 21%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429579B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-f6b7a8833b22409d8684a62ec3804fae |
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| Source note | uspto-grants-2008_09 |
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