HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → {2-[n-(Cyclohexylmethyl)-n-ethylamino]-7-fluoroquinolin-3-yl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57861258 | HCID 57861258 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | {2-[n-(Cyclohexylmethyl)-n-ethylamino]-7-fluoroquinolin-3-yl}methanol | HCID 57861244 | — |
Reaction Steps
To a mixture of 2-[N-(cyclohexylmethyl)-N-ethylamino]-7-fluoroquinoline-3-carbaldehyde (230 mg, 0.73 mmol) in ethanol (2 mL) is added sodium borohydride (30 mg, 0.79 mmol) and the mixture is stirred for 2 hours. After addition of sat. ammonium chloride and water, the mixture is extracted with ethyl acetate. The combined organic layer is washed with brine, dried over magnesium sulfate, filtered and concentrated to give [N-(cyclopentylmethyl)-N-ethylamino]quinolin-3-yl}methanol, which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410275B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-5eec75b9b8044723b15daa36284ad340 |
| Source note | uspto-grants-2013_04 |