HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-bromo-3-methoxypyrazine → HCID 18704806, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-bromo-3-methoxypyrazine | HCID 11344724 | — |
| Reactant | HCID 11463015 | HCID 11463015 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18704806 | HCID 18704806 | — |
Reaction Steps
The starting material 5-(N-benzyloxycarbonylamino)-N-(5-bromo-3-methoxy-2-pyrazinyl)-1-naphthalenesulphonamide was prepared using an analogous procedure to that described in Example 36, starting from proportionate amounts of 2-amino-5-bromo-3-methoxypyrazine and 5-(N-benzyloxycarbonylamino)-1-naphthalenesulphonyl chloride (obtained as described in Synlett., 1992, 661), in a yield of (11%; m.p. 226-228° C.; mass spectrum (+ve FAB, methanol/NBA): 543 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06083951 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-e1b5aebbbce642de900828a2018f7366 |
| Source note | uspto-grants-2000_07 |