HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(2-Amino-1-hydroxyethyl)benzene-1,3-diol → N-(4-{[4-(4-{[2-(2,4-Dihydroxyphenyl)-2-hydroxyethyl]amino}-1-piperidineyl)-anilino]sulfonyl}phenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(2-Amino-1-hydroxyethyl)benzene-1,3-diol | HCID 16768311 | — |
| Reactant | N-{4-[4-(4-Oxo-piperidin-1-yl)-phenylsulfamoyl]-phenyl}-acetamide | HCID 22220411 | — |
| Product | N-(4-{[4-(4-{[2-(2,4-Dihydroxyphenyl)-2-hydroxyethyl]amino}-1-piperidineyl)-anilino]sulfonyl}phenyl)acetamide | HCID 22220536 | — |
Reaction Steps
The title compound was prepared from N-{4-[4-(4-oxo-piperidine-1-yl)-phenylsulfamoyl]-phenyl}-acetamide (which was obtained in Example 216) and 2-amino-1-(2,4-dihydroxy-phenyl)-ethanol according to the procedure of Example 255 as a pale yellowish solid; 1H NMR (300 MHz, DMSO-d6) δ 1.55-1.75 (m, 2H), 1.95-2.15 (m, 2H), 2.08 (s, 3H), 2.50-3.20 (m, 5H), 3.60-3.70 (m, 2H), 5.04-5.10 (m, 1H), 6.65-6.75 (m, 1H), 6.24 (dd, J=8.1, 2.1 Hz, 1H), 6.32 (d, J=2.1 Hz, 1H), 6.80 (d, J=9.0 Hz, 2H), 6.88 (d, J=9.0 Hz, 2H), 7.12 (d, J=8.1 Hz, 1H), 7.59 (d, J=9.0 Hz, 2H), 7.70 (d, J=9.0 Hz, 2H), 9.26 (s, 1H), 9.71 (brs, 1H), 10.44 (s, 1H); MS (ES) m/z: 541.4 (MH+); HRMS Calcd. for C27H33N4O6S(MH+): 541.2121. Found: 541.2084.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06525202B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-5e603951944248b5b3a2ddd0587b5252 |
| Source note | uspto-grants-2003_02 |