HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Acetylsulfanilyl chloride → HCID 86627501, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Reactant | HCID 68937404 | HCID 68937404 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86627501 | HCID 86627501 | 38% |
Reaction Steps
This compound is prepared according to synthesis 43, from 60 mg (0.20 mmol) of 8-amino-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate hydrochloride (synthesis 64) and 50 mg (0.21 mmol) of 4-acetylamino-benzenesulfonyl chloride. After trituration in hot methanol, 35 mg (38%) of 8-(4-acetylamino-benzenesulfonylamino)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate is obtained in the form of an orange-brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426437B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-1ced3f229d4f44849f6950ea485e1133 |
| Source note | uspto-grants-2013_04 |