HuagongsheHuagongshe Chemistry Print Report · For research reference only
10-methoxymethyl-8-chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine → HCID 18670305, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 10-methoxymethyl-8-chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine | HCID 11335363 | — |
| Reactant | HCID 178478691 | HCID 178478691 | — |
| Product | HCID 18670305 | HCID 18670305 | 116% |
Reaction Steps
0.5 g of 10-methoxymethyl-8-chloromethyl-10H-pyrazino-[2,3-b][1,4]benzothiazine and 1.0 g of 4-(2-aminoethyl)imidazole dihydorchloride were treated by the same method as the one of Example 1094 to thereby give 0.7 g of crude 8-[4-(2-aminoethyl)imidazol-1-yl]-10-methoxymethyl-10H-pyrazino[2,3-b][1,4]benzothiazine as a brown solid. This crude product was then treated by the same method as the one of Example 316 to thereby give 0.1 g of N-[2-[1-(10-methoxymethyl-10H-pyrazino[2,3-b][1,4benzothiazin-8-ylmethyl)imidazol-4-yl]ethyl]methanesulfonamide. Further, it was treated by the same method as the one of Example 8 to thereby give 50 mg of the title compound as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518423B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-e9d0b59e605a435bb7a85e406ac015c8 |
| Source note | uspto-grants-2003_02 |