HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(6-amino-1,3-benzothiazol-2-yl)benzamide → N-[6-(Purin-6-ylamino)benzothiazol-2-yl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(6-amino-1,3-benzothiazol-2-yl)benzamide | HCID 810331 | — |
| Reactant | 6-Chloropurine | HCID 5359277 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[6-(Purin-6-ylamino)benzothiazol-2-yl]benzamide | HCID 23132486 | — |
Reaction Steps
N-[6-(Purin-6-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 6-chloropurine (29 mg, 0.186 mmol) in ethanol (3 ml) to 80° C. for 4 h. The resulting precipitate was separated by filtration and washed with ethanol (69 mg, 0.178 mmol, 96%). LC/ESI-MS: m/z 388 [M+H]+; m/z=386 [M−H]−; Rt=3.07 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576090B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-12504510e94a4259b7c77e7e1b9fe7be |
| Source note | uspto-grants-2009_08 |