HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamide → HCID 69655114, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamide | HCID 9837752 | — |
| Reactant | HCID 69655082 | HCID 69655082 | — |
| Product | HCID 69655114 | HCID 69655114 | — |
Reaction Steps
The title compound was prepared from 5-[4-(4-oxo-piperidin-1-yl)-benzylidene]-imidazolidine-2,4-dione (which was obtained in Example 42) and N-[5-(2-amino-1-hydroxy-ethyl)-2-hydroxy-phenyl]-methanesulfonamide (which was obtained in Example 9) according to the procedure of Example 73 as a pale yellowish solid; mp>201° C. (decomposed); 1H NMR (300 MHz, DMSO-d6) δ 1.20–1.40 (m, 2 H), 1.75–1.95 (m, 2 H), 2.50–2.90 (m, 5 H), 2.92 (s, 3 H), 3.70–3.85 (m, 2 H), 4.48 (dd, J=8.0, 4.2 Hz, 1 H), 6.33 (s, 1 H), 6.81 (d, J=8.1 Hz, 1 H), 6.95 (d, J=8.7 Hz, 2 H), 7.02 (dd, J=8.1, 1.8 Hz, 1 H), 7.18 (d, J=61.8 Hz, 1 H), 7.47 (d, J=8.7 Hz, 2 H); MS (ES) m/z: 516.1 (MH+); HRMS Calcd. for C24H30N5O6S (MH+): 516.1917. Found: 516.1922.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022716B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-d01ede53c05448ff9b2dd070f90006c4 |
| Source note | uspto-grants-2006_04 |