HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354205Generated: November 1, 2026
Sodium borohydride → HCID 21104611, compound
https://huagongshe.com/reaction/1354205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carbaldehyde | HCID 10773638 | — |
| Reactant | HCID 21104608 | HCID 21104608 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21104611 | HCID 21104611 | — |
Reaction Steps
Molecular sieve, type 3A, (1.082 g) and 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbaldehyde (0.095 g, 0.54 mmol) were added to a solution of (3S)-2-(3-aminomethyl-piperidin-1-yl)-1-(6-methoxy-quinolin-4-yl)-ethanol (0.171 g, 0.54 mmol) in MeOH (1.6 ml) and dichloromethane (3.8 ml). The reaction mixture was stirred at room temperature for 16 hours and sodium borohydride (0.054 g, 1.43 mmol) was added. The reaction mixture was stirred at room temperature for 2 hours and then filtered over Hydromatrix (wetted with an NaHCO3 solution, 2 ml) and subsequently washed with dichloromethane. The filtrate was concentrated to dryness by rotary evaporation. The residue was purified by column chromatography on silica gel (dichloromethane/MeOH 9/1 1% NH4OH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07223776B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-5f38059a67f647dc8b1faf166a3e2dc7 |
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| Source note | uspto-grants-2007_05 |
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