HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-(Pyridin-3-yl)-1H-imidazol-1-yl)butan-1-amine → 4-[4-(4-Pyrid-3-ylimidazol-1-yl)butylamino]-benzenesulfonic 2-(cyclopropanecarbonylamino)benzothiazol-6-yl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-(Pyridin-3-yl)-1H-imidazol-1-yl)butan-1-amine | HCID 11042160 | — |
| Reactant | 4-Fluorobenzenesulfonic acid 2-(cyclopropanecarbonylamino)-benzothiazol-6-yl ester | HCID 11523999 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 4-[4-(4-Pyrid-3-ylimidazol-1-yl)butylamino]-benzenesulfonic 2-(cyclopropanecarbonylamino)benzothiazol-6-yl ester | HCID 11541608 | — |
Reaction Steps
A solution of 4-fluorobenzenesulfonic 2-(cyclopropanecarbonylamino)benzo-thiazol-6-yl ester (example 7) (50 mg, 127.4 μmol) and 4-(4-pyrid-3-ylimidazol-1-yl)butylamine (110.2 mg, 0.51 mmol) in 0.5 ml of NMP is heated at 150° C. by microwave for 8 minutes. The crude reaction product is purified by preparative LC/MS (basic medium (pH 9)) to give after freeze-drying 36 mg of 4-(2-hydroxy-2-methylpropylamino)benzenesulfonic 2-(cyclo-propanecarbonylamino)benzothiazol-6-yl ester (beige-colored solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632952B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-addae98b79d54e2e9731d9f40046de6f |
| Source note | uspto-grants-2009_12 |