HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Piperidinyl)-1,3-benzoxazol-2(3H)-one → HCID 19085834, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Piperidinyl)-1,3-benzoxazol-2(3H)-one | HCID 11321928 | — |
| Reactant | HCID 19085855 | HCID 19085855 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19085834 | HCID 19085834 | — |
Reaction Steps
From 4-(2-oxo-3-benzoxazolinyl)-piperidine and 2-(4-hydroxybutyl)-1,1-dioxido-5-(2-propyl)-1,2-benzothiazol-3(2H)-one using the procedure described for Example 66, Steps 4-6 there was obtained a white solid: 1H NMR (400 MHz, CDCl3) 7.9 (s, 1H), 7.8 (d, 1H), 7.7 (d, 1H), 7.3 (m, 1H), 7.2-7.0 (br m, 3H), 4.2 (m, 1H), 3.8 (m, 2H), 3.1 (m, 3H), 2.7-2.5 (br m, 2H), 2.1 (m, 2H), 2.0-1.8 (br m, 4H), 1.7-1.6 (m, 4H), 1.35 (d, 6H) Analysis calculated for C25H30 N3O6S·HCl·1.6 CH3CO2CH2CH3 C: 57.64, H: 6.69, N: 6.23 found C: 57.06, H: 6.12, N: 6.56.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760054 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-bc2fefa06bf64058a0fec13fa6b7878d |
| Source note | uspto-grants-1998_06 |