HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(Aminosulfonyl)benzoate → HCID 73053706, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(Aminosulfonyl)benzoate | HCID 4652880 | — |
| Reactant | HCID 19029914 | HCID 19029914 | — |
| Product | HCID 73053706 | HCID 73053706 | — |
Reaction Steps
The compound was prepared according to GP-2 using 2-sulfamoylbenzoic acid ethyl ester 4 and compound 3a. The crude product was purified by flash column chromatography using MeOH—CHCl3 to obtain 5a. 1H NMR (500 MHz, DMSO-d6) δ 9.43 (bs, 2H), 8.49-8.46 (m, 4H), 7.87 (t, J=8.0 Hz, 2H), 7.68 (d, J=7.5 Hz 1H), 7.64 (d, J=8.0 Hz 1H), 7.49 (t, J=7.5 Hz, 1H), 7.33 (t, J=7.5 Hz, 1H), 4.02 (t, J=7.5, 2H), 2.76 (q, J=7.0 Hz, 2H), 1.90-1.60 (m, 2H). MS (ES−) m/z 437 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056835B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-ebcf33e6cef345fcb56a7f2d45cbce71 |
| Source note | uspto-grants-2015_06 |