HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061379Generated: November 2, 2026
HCID 12051793, compound → HCID 69654943, compound
https://huagongshe.com/reaction/1061379
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 12051793 | HCID 12051793 | — |
| Reactant | N-{4-[4-(4-Oxo-piperidin-1-yl)-phenylsulfamoyl]-phenyl}-acetamide | HCID 22220411 | — |
| Product | HCID 69654943 | HCID 69654943 | — |
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 (2S)-3-(9H-carbazol-4-yloxy)-2-hydroxy-propylamine (Berridge et al., Int. J. Radial. Appl. Instrum., 1992, 563) according to the procedure of Example 255 as a yellowish solid; 1H NMR (300 MHz, DMSO-d6) δ 1.55-1.75 (m, 2H), 2.00-2.15 (m, 2H), 2.06 (s, 3H), 2.50-2.70 (m, 2H), 3.00-3.50 (m, 3H), 3.60-3.70 (m, 2H), 4.10-4.25 (m, 2H), 4.35-4.50 (m, 1H), 5.97 (brs, 1H), 6.72 (d, J=8.0 Hz, 1H), 6.80 (d, J=8.0 Hz, 2H), 6.88 (d, J=8.0 Hz, 2H), 7.10-7.50 (m, 5H), 7.59 (d, J=8.7 Hz, 2H), 7.69 (d, J=8.7 Hz, 2H), 8.22 (d, J=7.8 Hz, 1H), 9.71 (s, 1H), 10.40 (s, 1H), 11.32 (s, 1H); MS (ES) m/z: 627.9 (MH+); HRMS Calcd. for C34H38N5O5S(MH+): 628.2594. Found: 628.2593.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06525202B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-f154048318c2437fb0d3663710087e1c |
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| Source note | uspto-grants-2003_02 |
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