HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloropropanesulphonyl chloride → [4-(2,4-Dicyclopropylphenyl)piperazin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloropropanesulphonyl chloride | HCID 15410 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | HCID 58484588 | HCID 58484588 | — |
| Reactant | HCID 71252153 | HCID 71252153 | — |
| Product | [4-(2,4-Dicyclopropylphenyl)piperazin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanone | HCID 71251931 | — |
Reaction Steps
Using [4-(2,4-dicyclopropylphenyl)piperazin-1-yl](6-fluoro-4-methylpyridin-3-yl)methanone (480 mg) described in Preparation Example 179, 4-methoxybenzylamine (2 mL) and 3-chloropropane-1-sulfonyl chloride (0.31 mL) and by the reaction and treatment in the same manner as in Example 229, the title compound (450 mg) was obtained via (6-amino-4-methylpyridin-3-yl)[4-(2,4-dicyclopropylphenyl)piperazin-1-yl]methanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08816079B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-4d2bbcfda41c496780a3b683aaf9bee7 |
| Source note | uspto-grants-2014_08 |