HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373951Generated: November 3, 2026
Sodium borohydride → HCID 21075799, compound
https://huagongshe.com/reaction/1373951
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21075800 | HCID 21075800 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21075799 | HCID 21075799 | 88.1% |
Reaction Steps
A solution of N-(7-bromo-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)isopropylideneamine (18.4 g, 53.3 mmol) in 100 mL of methanol was placed under an atmosphere of nitrogen and cooled in an ice water bath. The solution was treated with sodium borohydride (2.32 g, 61.3 mmol) over 30 min. The reaction mixture was allowed to slowly come to ambient temperature. After 1.5 h, the reaction was quenched by the addition of 25 mL of saturated NH4Cl solution. The reaction mixture was concentrated under reduced pressure to remove the methanol. The residue was partitioned between chloroform (150 mL) and 10% Na2CO3 solution (35 mL), and the phases were separated. The organic portion was washed with another portion of 10% Na2CO3 solution (35 mL), water (35 mL) and brine (35 mL). The organic portion was dried over Na2SO4, filtered and concentrated under reduced pressure to yield a brown foam. The foam was purified by chromatography (SiO2, 97:3 CHCl3:MeOH gradient to 9:1) to give 16.3 g of N-(7-bromo-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)isopropylamine as a dark tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163947B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-2d6dedb274154293a4d53576cf7bf754 |
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| Source note | uspto-grants-2007_01 |
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