HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856479Generated: October 27, 2026
Sodium borohydride → HCID 69521947, compound
https://huagongshe.com/reaction/856479
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86595183 | HCID 86595183 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69521947 | HCID 69521947 | 71.5% |
Reaction Steps
7-[4-(2-butoxyethoxy)phenyl]-N-[4-[[(1-oxido-2-pyridinyl)sulfonyl]methyl]phenyl]-1-(trifluoroacetyl)-2,3-dihydro-1-benzazepine-4-carboxamide (137 mg) was dissoved in ethanol (4.0 ml), sodium borohydride (36 mg) was added to the mixture, and the mixture was stirred at room temperature for 3 hours. Sodium borohydride (36 mg) was further added to the mixture, and the mixture was stirred at room temperature for 3 hours. The solvent was removed under reduced pressure and the obtained residue was added to water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give 7-[4-(2-butoxyethoxy)phenyl]-N-[4-[[(1-oxido-2-pyridinyl)sulfonyl]methyl]phenyl]-2,3-dihydro-1-benzazepine-4-carboxamide (Compound 202) (85 mg).
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-8827b8a644724baa963296a0e6fe1ed0 |
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| Source note | uspto-grants-2007_08 |
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