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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273253Generated: October 30, 2026

Hydrazine hydrate (1:1) → HCID 178487810, compound

https://huagongshe.com/reaction/2273253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 178487809HCID 178487809—
SolventEthanolHCID 702—
ProductHCID 178487810HCID 178487810135.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

Hydrazine hydrate (2M solution in methanol, 90 μL, 0.18 mmol, 1.0 eq) is added at room temperature to a stirred solution of 2-[trans-4-(6-methoxy-4-methyl-3,4-dihydro-2H-1-oxa-4,5,9-triaza-phenanthren-3-yl)-cyclohexyl]-isoindole-1,3-dione (105 mg, 0.18 mmol, 1.0 eq) in ethanol (3 mL). After 16 hours stirring at 50° C., solvent is removed to afford trans-4-(6-methoxy-4-methyl-3,4-dihydro-2H-1-oxa-4,5,9-triaza-phenanthren-3-yl)-cyclohexylamine as an orange semisolid (80 mg, 93% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120822B2
Source datasetuspto-grants-2015_09
ORD IDord-30162a378f4d49ea984eb3670cf99a97
Source noteuspto-grants-2015_09