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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422934Generated: October 30, 2026

HCID 178487815, compound → HCID 178487813, compound

https://huagongshe.com/reaction/1422934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178487815HCID 178487815—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178487813HCID 17848781374%

Reaction Conditions

Temperature40 °C

Reaction Steps

10% Palladium on activated carbon (285 mg, 2.68 mmol, 1.0 eq) is added at room temperature to a stirred solution of [trans-4-(6-methoxy-3,4-dihydro-2H-1-oxa-4,5,9-triaza-phenanthren-3-yl)-cyclohexyl]-carbamic acid benzyl ester (1.20 g, 2.68 mmol, 1.0 eq) in methanol (80 mL) and tetrahydrofuran (8 mL). The resulting mixture is stirred under hydrogen flow (1 bar) at 40° C. for 16 hours. The catalyst is then removed by filtration and the solution is concentrated to afford trans-4-(6-methoxy-3,4-dihydro-2H-1-oxa-4,5,9-triaza-phenanthren-3-yl)-cyclohexylamine as a yellow solid (620 mg, 74% yield) which is directly engaged in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927541B2
Source datasetuspto-grants-2015_01
ORD IDord-8abf2011de79462b843b99a163406ca7
Source noteuspto-grants-2015_01