HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757576Generated: October 28, 2026
Sodium borohydride → 6-Methyl-N4-(2-methylpropyl)-N2, N2-bis(phenylmethyl)pyridine-2,3,4-triamine
https://huagongshe.com/reaction/1757576
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-methyl-N4-(2-methylpropyl)-3-nitro-N2, N2-bis(phenylmethyl)pyridine-2,4-diamine | HCID 54093023 | — |
| Catalyst | Nickel chloride hydrate | HCID 16212333 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Methyl-N4-(2-methylpropyl)-N2, N2-bis(phenylmethyl)pyridine-2,3,4-triamine | HCID 53881272 | 85.1% |
Reaction Steps
Sodium borohydride (585 mg, 16 mmole) was added to a solution of nickel (II) chloride hydrate (1.02 g, 4.3 mmole) in methanol (100 mL). The addition caused a black solid to form along with gas evolution. The resulting heterogeneous mixture was stirred at ambient temperature for 30 minutes. A solution containing 6-methyl-N4 -(2-methylpropyl)-3-nitro-N2, N2 -bis(phenylmethyl)pyridine-2,4-diamine (3.47 g, 8.6 mmole) in methylene chloride (20 mL) was added followed by the addition of sodium borohydride (1.37 g, 36 mmole). The reaction mixture was stirred at ambient temperature for about 30 minutes then eluted through a layer of silica gelwith a methanol/methylene chloride mixture. The filtrate was concentrated under vacuum. The resulting residue was partitioned between ethyl acetate and water. The ethyl acetate layer was separated, dried with magnesium sulfate and concentrated under vacuum to provide 2.74 g of the desired product as a green foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05446153 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-c3cd4a12cc5a41c396a2f0862c202ced |
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| Source note | uspto-grants-1995_08 |
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