HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Acetylsulfanilyl chloride → HCID 86734629, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Reactant | HCID 15218124 | HCID 15218124 | — |
| Reactant | HCID 86734630 | HCID 86734630 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86734629 | HCID 86734629 | — |
Reaction Steps
A mixture of 1.53 g. of 1-ethyl-5-methylcytosine, 2.34 g. of N-acetylsulfanilyl chloride and 10 ml. of pyridine was stirred overnight, diluted with 100 ml. of cold water, filtered with a little Hyflo to remove turbidity and acidified by addition of 19 ml. of 6N hydrochloric acid. The product was allowed to crystallize for several hours at room temperature before filtering, washing with water, and drying in a vacuum desiccator over potassium hydroxide to obtain 1.78 g. of N4 -acetyl-N1 -(1-ethyl-1,2-dihydro-5-methyl-4-pyrimidinyl)-sulfanilamide, melting at 235°-239°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04016267 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-a0952716119046c8a731337e1f0b7350 |
| Source note | uspto-grants-1977_04 |