HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-{4-[(5,5-Dioxido-2,3-dihydro-1h-pyrrolo[2,1-c][1,2,4]benzothiadiazin-7-yl)oxy]phenyl}-n'-hydroxyethanimidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | {4-[(5,5-Dioxido-2,3,3a,4-tetrahydro-1H-pyrrolo[2,1-c][1,2,4]benzothiadiazin-7-yl)oxy]phenyl}acetonitrile | HCID 69199240 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-{4-[(5,5-Dioxido-2,3-dihydro-1h-pyrrolo[2,1-c][1,2,4]benzothiadiazin-7-yl)oxy]phenyl}-n'-hydroxyethanimidamide | HCID 87871618 | — |
Reaction Steps
2.51 ml (18.0 mmol) of triethylamine are added to a solution of 1.25 g (18.0 mmol) of hydroxylamine hydrochloride in 4 ml of DMSO and the suspension is stirred for 10 minutes. The precipitate is filtered off and the filtrate is concentrated. 992 mg (3.00 mmol) of the product of Step A of Example 27 are added to the filtrate and the solution is stirred at 75° C. for 1 hour 30 minutes. The solution is allowed to return to ambient temperature, and precipitation of the reaction mixture is brought about using water. The precipitate is filtered off to yield the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253162B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-baace91d42e7404c859bed8af6fb546b |
| Source note | uspto-grants-2007_08 |