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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519063Generated: October 30, 2026

HCID 86727378, compound → HCID 76287822, compound

https://huagongshe.com/reaction/519063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86727378HCID 86727378—
CatalystPalladium hydroxideHCID 9942167—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 76287822HCID 76287822139.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 6-(1-benzhydryl-3-methyl-azetidin-3-ylamino)-4-methyl-7-phenyl-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one (Example #79, Step C, 0.10 g, 0.18 mmol) in THF (20 mL), MeOH (20 mL) and aqueous HCl (12N, 0.3 mL) was added Pd(OH)2/C (10%, 0.02 g, 0.014 mmol) and the solution was heated at 50° C. under an atmosphere of H2 (55 psi) for 4 h. The reaction mixture was cooled to ambient temperature and filtered. The filtrate was evaporated in vacuo to give 4-methyl-6-(3-methyl-azetidin-3-ylamino)-7-phenyl-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one (0.095 g, 57% pure, 82%), which was used in the next step directly without further purification. LC/MS (Table 1, Method 2) Rt=0.890 min; MS m/z: 378 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-410bc7a303964d77ac4eebd9a71d08c8
Source noteuspto-grants-2015_08