HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415552Generated: October 28, 2026
Sodium borohydride → HCID 86633743, compound
https://huagongshe.com/reaction/415552
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86633744 | HCID 86633744 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 86633743 | HCID 86633743 | 93.7% |
Reaction Steps
Sodium borohydride (110 mg, 2.8 mmol) was added to a solution of nickel (II) chloride hexahydrate (330 mg, 1.4 mmol) in 10 mL of methanol. A solution of benzyl (3R)-3-[(3-nitroquinolin-4-yl)amino]butylcarbamate (1.11 g, 2.81 mmol) in 20 mL of 1:1 methanol/dichloromethane was added, and the resulting dark mixture was stirred for 5 minutes at room temperature. Additional sodium borohydride was added in small portions until the reaction solution become colorless. The mixture was filtered through a layer of CELITE filter agent, and the filtrate was concentrated under reduced pressure. The resulting brown solid was triturated with dichloromethane, and the resulting mixture was filtered through a layer of CELITE filter agent. The filtrate was concentrated under reduced pressure to provide 0.96 g of benzyl (3R)-3-[(3-aminoquinolin-4-yl)amino]butylcarbamate as a brown foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088788B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-3df0586a16d44b379b47b31a6480d3df |
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| Source note | uspto-grants-2012_01 |
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