HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Furanmethanol → 3-Fluoro-N-[4-(3-furylmethoxy)-1-naphthyl]-5-piperidin-1-ylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Furanmethanol | HCID 20449 | — |
| Reactant | tert-Butyl (4-hydroxynaphthalen-1-yl)carbamate | HCID 10923237 | — |
| Reactant | 3-Fluoro-5-piperidinylbenzoic acid | HCID 59553180 | — |
| Product | 3-Fluoro-N-[4-(3-furylmethoxy)-1-naphthyl]-5-piperidin-1-ylbenzamide | HCID 59553349 | — |
Reaction Steps
Compound is prepared from tert-butyl (4-hydroxy-1-naphthyl)carbamate, 3-fluoro-5-piperidin-1-yl-benzoic acid and furan-3-yl-methanol according to conditions described in general procedure D. A pink solid is produced (12 mg). Mp: 152-153° C.; 1H NMR (300 MHz, CDCl3) δ 1.63-1.69 (m, 6H), 3.20-3.27 (m, 2H), 5.13 (s, 2H), 6.58 (s, 1H), 6.75 (d, J=12.6 Hz, 1H), 6.89 (d, J=8.4 Hz, 1H), 6.98 (d, J=9.0 Hz, 1H), 7.30 (s, 1H), 7.47-7.59 (m, 4H), 7.12 (d, J=8.1Hz, 1H), 7.83 (d, J=8.4 Hz, 1H), 7.95 (s, 1H), 8.32 (d, J=8.1Hz, 1H); MS 445 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829560B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-32e0ed3acc01423193cb70f7569e1104 |
| Source note | uspto-grants-2010_11 |