HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Chloro-3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-5-(naphthalen-2-ylsulfonylcarbamoyl)benzoic acid → HCID 71062203, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Chloro-3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-5-(naphthalen-2-ylsulfonylcarbamoyl)benzoic acid | HCID 71062145 | — |
| Reactant | HCID 71062313 | HCID 71062313 | — |
| Product | HCID 71062203 | HCID 71062203 | 85% |
Reaction Steps
Following a procedure analogous to that for the synthesis of Intermediate 91F, ethyl 2-(4-chloro-3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-5-(1-(3,4-dichlorobenzyl)indolin-5-ylsulfonylcarbamoyl)benzoate (355 mg, 0.44 mmol) was converted to the title compound (290 mg, 85%). 1H NMR (DMSO-d6) δ 8.14 (d, J=2.0 Hz, 1H), 8.17 (dd, J=8.3, 2.1 Hz, 1H), 7.69-7.57 (m, 5H), 7.32-7.30 (m, 1H), 6.65 (d, J=8.6 Hz, 1H), 4.45 (s, 2H), 3.53 (t, J=8.7 Hz, 2H), 3.40-3.28 (m, 4H), 3.05 (t, J=8.4 Hz, 2H), 2.11 (s, 3H), 1.56-1.41 (m, 4H), 1.33-1.27 (m, 2H), 1.15-1.08 (m, 2H), 0.91 (t, J=7.3 Hz, 3H), 0.74 (t, J=7.4 Hz, 3H); MS(ESI+) m/z 776.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346795B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-3666a38905a0484dbc57cdd25c31f977 |
| Source note | uspto-grants-2016_05 |