HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620233Generated: October 31, 2026
Sodium borohydride → (2-(Isopropylamino)-6-methoxyquinolin-3-yl)methanol
https://huagongshe.com/reaction/1620233
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(Isopropylamino)-6-methoxyquinoline-3-carbaldehyde | HCID 86669820 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-(Isopropylamino)-6-methoxyquinolin-3-yl)methanol | HCID 68182178 | 93% |
Reaction Steps
To a stirred solution of 2-(isopropylamino)-6-methoxyquinoline-3-carbaldehyde SLA 28186 (1.55 g, 6.35 mmol) in THF (100 mL) in a 250 mL round-bottomed flask equipped with a magnetic stirrer was added NaBH4 (0.24 g, 6.35 mmol) and the mixture was stirred for overnight at RT then cooled in an ice bath before quenching by addition of a 1 N aq. HCl solution (40 mL). After stirring for 15 min at that temperature, the mixture was basified to pH=9 with a 2 N aq. NaOH solution. THF was removed at 40° C. under vacuum and the solution was extracted with CH2Cl2 (200 mL). The organic layer was washed with brine (20 mL), dried over Na2SO4, filtered, and concentrated under vacuum to give (2-(isopropylamino)-6-methoxyquinolin-3-yl)methanol SLA 28188 as an orange solid (1.45 g, 93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772316B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-a8f0cab22aeb4c869cd609cc65170cd1 |
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| Source note | uspto-grants-2014_07 |
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