HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-(-)-Tetrahydrofurfurylamine → HCID 178441276, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-(-)-Tetrahydrofurfurylamine | HCID 2734124 | — |
| Reactant | HCID 178441278 | HCID 178441278 | — |
| Product | HCID 178441276 | HCID 178441276 | — |
Reaction Steps
The product from Example 173 and (R)-(tetrahydrofuran-2-yl)methanamine (Aldrich) were processed using the method described in Example 178 to afford the title compound. 1H NMR (DMSO-d6) δ 0.48 (s, 3H), 0.90 (t, J=7.3 Hz, 3H), 1.19 (s, 3H), 1.24 (s, 3H), 1.26-1.52 (m, 5H), 1.57 (s, 9H), 1.57-1.67 (m, 2H), 1.74-1.89 (m, 3H), 1.95-2.08 (m, 1H), 2.62-2.83 (m, 4H), 2.91-2.99 (m, 1H), 3.22-3.33 (m, 2H), 3.56-3.84 (m, 2H), 7.58-7.62 (m, 1H), 8.50 (s, 1H). (ESI+) m/z 478 (M+H)+. Anal. calcd. for C26H43N3O3S: C, 65.37; H, 9.07; N, 8.80. Found: C, 65.39; H, 8.91; N, 8.66.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501794B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-a4d74fd65be74dd1addd6a43ee670b71 |
| Source note | uspto-grants-2013_08 |