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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863954Generated: November 4, 2026

HCID 57973773, compound → HCID 11589768, compound

https://huagongshe.com/reaction/1863954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57973773HCID 57973773—
ReactantHCID 57973796HCID 57973796—
Solvent2-MethoxyethanolHCID 8019—
ProductHCID 11589768HCID 11589768—

Reaction Steps

A mixture of 208 mg (0.6 mmol) of of tert-butyl[(1R)-3-hydrazino-3-oxo-1-(2,4,5-trifluorobenzyl)propyl]carbamate (Intermediate 4), 100 mg (0.45 mmol) of 2-(trifluoromethyl)-6,7-dihydro[1,2,4]triazolo[1,5-a]pyrazine-8(5H)-thione (Intermediate 7), and 5 mL of 2-methoxyethanol was stirred at reflux for 18 h, resulting primarily in ring closure of the initial adduct as well as loss of the Boc group. The cooled solution was purified by preparative HPLC (C18 reverse phase column, 30-75% acetonitrile in water containing 0.05% trifluoroacetic acid) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625888B2
Source datasetuspto-grants-2009_12
ORD IDord-0478d6bd60f84a1caf4314db5c0fd9e2
Source noteuspto-grants-2009_12