HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 6-{1-[(3-Methylbutylamino)methyl]isoquinolin-4-yloxy}nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Isoamylamine | HCID 7894 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 6-(1-Formylisoquinolin-4-yloxy)nicotinamide | HCID 59401314 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 6-{1-[(3-Methylbutylamino)methyl]isoquinolin-4-yloxy}nicotinamide | HCID 25121480 | — |
Reaction Steps
To 6-(1-formylisoquinolin-4-yloxy)nicotinamide (Preparation 20) (130 mg, 0.44 mmol) in dichloroethane (8 mL) was added 3-methylbutylamine (154 μL, 1.33 mmol), NaBH(OAc)3 (282 mg, 1.33 mmol) and acetic acid (76 μL, 1.33 mmol). The mixture was stirred for 16 h. NaHCO3 (50 mL) was added and the mixture extracted with EtOAc (3×40 mL). The organic phase was washed with water (30 mL), brine (30 mL) and dried (MgSO4). Solvent was removed in vacuo and the residue purified by column chromatography (0.5 NH3: 5 MeOH: 95 DCM) to give the title compound: RT=2.48 min; m/z (ES+)=365.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278442B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-130144816ffc4650bbc2d6510b1d6fee |
| Source note | uspto-grants-2012_10 |