HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856387Generated: October 29, 2026
HCID 11238707, compound → HCID 3013419, compound
https://huagongshe.com/reaction/856387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11238707 | HCID 11238707 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 3013419 | HCID 3013419 | 146.2% |
Reaction Steps
7-[4-(2-butoxyethoxy)phenyl]-N-[4-[hydroxy(4-methyl-1-oxidopyridin-2-yl)methyl]phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxamide (0.25 g) and isobutylaldehyde (0.15 ml) were dissolved in 1,2-dichloroethane (80 ml), and to the solution, triacetoxy sodium borohydride (0.27 g) was added under ice-cooling and the mixture was stirred overnight at room temperature. To the mixture, isobutylaldehyde (1 ml) and triacetoxy sodium borohydride (1.3 g) were further added, and the mixture was stirred overnight at room temperature. The mixture was washed with sodium bicarbonate solution and water, and dried over anhydrous magnesium sulfate. The solvent was distilled off, to give 7-[4-(2-butoxyethoxy)phenyl]-N-[4-[hydroxy(4-methyl-1-oxidopyridin-2-yl)methyl]phenyl]-1-isobutyl-2,3-dihydro-1H-1-benzazepine-4-carboxamide (compound 2) (0.2 g) as yellow amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262185B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-c78f7329aa8241b69e90be87bd17242b |
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| Source note | uspto-grants-2007_08 |
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