HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Ammonia dichloromethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Isopropylpiperazine | HCID 78013 | — |
| Reactant | 4-(3-Piperidin-1-ylpropoxy)benzaldehyde | HCID 2766324 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Isopropyl-4-[4-(3-piperidin-1-yl-propoxy)-benzyl]-piperazine | HCID 10155403 | — |
| Product | Ammonia dichloromethane | HCID 22731429 | 1% |
Reaction Steps
A solution of the product of Example 9 (200 mg), 1-isopropyl-piperazine (100 mg), and acetic acid (0.05 mL) in DCM (3 mL) was treated with sodium triacetoxyborohydride (290 mg). After 16 h, the resulting mixture was treated with 10% sodium hydroxide (5 mL) and extracted with DCM (3×10 mL). The combined organic phases were dried (sodium sulfate) and evaporated. Chromatography of the residue (1-5% 2 M methanolic ammonia/DCM) gave the title compound as a colorless oil (225 mg). 1H NMR (400 MHz, CDCl3): 7.19 (d, J=8.6 Hz, 2H), 6.83 (d, J=8.6 Hz, 2H), 3.98 (t, J=6.6 Hz, 2H), 3.43 (s, 2H), 2.63 (m, 1H), 2.53 (br, 4H), 2.46 (m, 4H), 2.39 (br, 4H), 1.96 (m, 2H), 1.58 (m, 4H), 1.46-1.40 (m, 2H), 1.03 (d, J=6.5 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429586B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-59ed4c5836a74af7b0dc4532aaac0233 |
| Source note | uspto-grants-2008_09 |