HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 4-{4-[(7-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-butyl}-[1,4]oxazepan-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 7-methoxy-N-propyl-1,2,3,4-tetrahydronaphthalen-2-amine | HCID 10082172 | — |
| Reactant | 4-(6-Oxo-[1,4]oxazepan-4-yl)-butyraldehyde | HCID 22640253 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-{4-[(7-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-butyl}-[1,4]oxazepan-5-one | HCID 12110052 | — |
Reaction Steps
To (7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amine (ca.13 mg 50 μmole) prepared as described in Example 1, was added 440 μL solution of 4-(6-oxo-[1,4]oxazepan-4-yl)-butyraldehyde (0.125 M in 1,2 dichloroethane), 30 μL diisopropylethylamine (DIEA) and 300 μL of 0.25 M slurry of sodium triacetoxyborohydride in 1,2 dichloroethane. The reaction was shaken at room temperature for 48 h. After quenching with 2 mL 2% NaOH, the reaction mixture was transferred along with 0.5 mL water and ethyl acetate to workup flasks. The organic phase was washed, dried and concentrated. Purification by chromatography yielded 3-{4-[(7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-butyl}-[1,3]oxazinan-2-one 18, MS: 375 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818645B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-a6c8ec35fc9647ecb45ef47f60faeaf3 |
| Source note | uspto-grants-2004_11 |