HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N-{6-[4-(4-Methylpiperazin-1-yl)pyrimidin-2-ylamino]benzothiazol-2-yl}benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | N-(6-amino-1,3-benzothiazol-2-yl)benzamide | HCID 810331 | — |
| Reactant | 2-Chloro-4-(4-methylpiperazin-1-yl)pyrimidine | HCID 1714225 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-{6-[4-(4-Methylpiperazin-1-yl)pyrimidin-2-ylamino]benzothiazol-2-yl}benzamide | HCID 23132480 | — |
Reaction Steps
N-{6-[4-(4-Methylpiperazin-1-yl)pyrimidin-2-ylamino]benzothiazol-2-yl}benzamide was prepared by heating a mixture of N-(6-aminobenzothiazol-2-yl)benzamide (IM 2, 50 mg, 0.186 mmol) and 2-chloro-4-(4methylpiperazin1-yl)pyrimidine (IM 10, 40 mg, 0.186 mmol) in ethanol (3 mL) to 80° C. for 4 days. After dissolving the precipitate by addition of dimethylformamide, pTLC (dichloromethane:methanol=4.1) yielded a solid (44 mg, 0.100 mmol, 54%). LC/ESI-MS: m/z=446 [M+H]+; m/z=444 [M−H]−; Rt=2.12 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576090B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-59a2a14b3c344cafb1c03889e0e253c4 |
| Source note | uspto-grants-2009_08 |