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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343391Generated: October 29, 2026

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

https://huagongshe.com/reaction/343391

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromo-3-methoxypyrazineHCID 11344724—
ReactantHCID 11463015HCID 11463015—
SolventMethanolHCID 887—
ProductHCID 18704806HCID 1870480611%

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 (H+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861401
Source datasetuspto-grants-1999_01
ORD IDord-191977d039ab43238c88d2276ce60f70
Source noteuspto-grants-1999_01