HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide → HCID 69654864, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide | HCID 12047933 | — |
| Reactant | HCID 69655037 | HCID 69655037 | — |
| Product | HCID 69654864 | HCID 69654864 | — |
Reaction Steps
The title compound was prepared from 3-[4-(4-oxo-piperidine-1-yl)-phenylsulfamoyl]-thiophene-2-carboxylic acid methyl ester (which was obtained in Example 234) and N-[5-((1R)-2-amino-1-hydroxy-ethyl)-2-hydroxy-phenyl]-methanesulfonamide (which was obtained in Example 10) according to the procedure of Example 278 as a pale yellowish solid; 1H NMR (300 MHz, DMSO-d6) δ 1.20-1.40 (m, 2H), 1.70-1.90 (m, 2H), 2.50-2.75 (m, 5H), 3.40-3.55 (m, 2H), 3.89 (s, 2H), 4.46 (dd, J=8.0, 4.2 Hz, 1H), 6.75-6.85 (m, 3H), 6.90 (d, J=9.0 Hz, 2H), 7.00 (dd, J=8.3, 2.0 Hz, 1H), 7.16 (d, J=2.0 Hz, 1H), 7.32 (d, J=3.3 Hz, 1H), 7.89 (d, J=3.3 Hz, 1H); MS (ES) m/z: 624.9 (MH+); HRMS Calcd. for C26H34N4O8S3 (MH+): 625.1455. Found: 625.1441.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06525202B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-5b2bf803f8ff4a428d263ccbcd49b28a |
| Source note | uspto-grants-2003_02 |