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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287403Generated: October 29, 2026

2-Amino-5-bromo-3-methoxypyrazine → HCID 18704806, compound

https://huagongshe.com/reaction/2287403

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromo-3-methoxypyrazineHCID 11344724—
ReactantHCID 11463015HCID 11463015—
SolventMethanolHCID 887—
ProductHCID 18704806HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083951
Source datasetuspto-grants-2000_07
ORD IDord-e1b5aebbbce642de900828a2018f7366
Source noteuspto-grants-2000_07