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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827693Generated: October 30, 2026

Methanol → HCID 486241, compound

https://huagongshe.com/reaction/1827693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium hydrideHCID 24758—
ReactantPhenoxazineHCID 67278—
Reactant6-(Bromomethyl)-2-imino-2,3-dihydropteridin-4-amine--hydrogen bromide (1/1)HCID 12503242—
SolventTetrahydrofuranHCID 8028—
ProductHCID 486241HCID 486241—

Reaction Steps

NaH (60% oil suspension containing 51 mg, 2.0 mmol) was added to a stirred solution of phenoxazine (147 mg, 0.784 mmol) in dry THF (10 mL) at 0° C. under N2. After 10 min. 2,4-diamino-6-bromomethylpteridine hydrobromide (100 mg, 0.392 mmol) was added and the reaction mixture was allowed to come to room temperature and left to stir for 2 days. The excess NaH was decomposed with MeOH (1 mL), and the mixture was concentrated to dryness by rotary evaporation. Flash chromatography on silica gel yielded the title compound, N-[(2,4-diaminopteridin-6-yl)methyl]phenoxazine, as a brown solid; yield 47 mg (34%); mp >250° C. dec. Anal. Calcd. for C19H15N7O0.4H2O: C, 62.60; H, 4.37. Found: C, 62.84; H, 4.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056911B1
Source datasetuspto-grants-2006_06
ORD IDord-b628f74a68624ca08b46c92469beeb03
Source noteuspto-grants-2006_06