HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(2,5-Dichloro-3-methanesulfonyl-indol-1-yl)-acetimidic acid ethyl ester hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | (2,5-Dichloro-3-methylsulfonyl-indol-1-yl)-acetonitrile | HCID 22574012 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(2,5-Dichloro-3-methanesulfonyl-indol-1-yl)-acetimidic acid ethyl ester hydrochloride | HCID 69546225 | 91% |
Reaction Steps
A solution of (2,5-dichloro-3-methylsulfonyl-indol-1-yl)-acetonitrile (0.303 g, 1 mmole) in dry chloroform (15 ml) was cooled to 0° C. under a nitrogen atmosphere. To this solution was added anhydrous ethanol (0.35 ml). Dry hydrogen chloride gas was bubbled into the reaction mixture to saturation at 0° C. The flask was stoppered and stirred for 2 h at 0 and left in the freezer overnight. The resulting white solid precipitate was filtered off and dried to afford 0.353 g (91%) of 2-(2,5-dichloro-3-methanesulfonyl-indol-1-yl)-acetimidic acid ethyl ester hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852726B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-d94932f83a294bdbab27330a23d11799 |
| Source note | uspto-grants-2005_02 |