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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923631Generated: October 31, 2026

Tetrahydrofuran → 6-(aminomethyl)-2-phenylquinazolin-4(3H)-one

https://huagongshe.com/reaction/923631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 136636244HCID 136636244—
CatalystCobalt(II) chloride hydrateHCID 16211468—
SolventMethanolHCID 887—
Product6-(aminomethyl)-2-phenylquinazolin-4(3H)-oneHCID 13663624556%

Reaction Steps

Prepared from INT-87. To a stirring solution of 4-oxo-2-phenyl-3,4-dihydroquinazoline-6-carbonitrile INT-87 (540 mg, 2.18 mmol) in MeOH (30 mL) and THF (10 mL) was added cobalt(II) chloride hydrate (646 mg, 4.37 mmol) and sodium borohydride (826 mg, 21.8 mmol) portionwise. After stirring at room temperature for 30 min the reaction mixture was quenched with 1 M HCl (5 mL) and filtered through a celite plug, washing with THF (50 mL). The mixture was diluted with EA (100 mL) and washed with NaHCO3 (120 mL) and brine (20 mL). The organics were dried over MgSO4 and concentrated in vacuo to afford 306 mg (56%) of 6-(aminomethyl)-2-phenylquinazolin-4(3H)-one INT-88 as a white powder. LCMS-ESI (m/z) calculated for C15H13N3O: 251; found 250 [M−H]−, tR=0.80 min (Method 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278910B2
Source datasetuspto-grants-2016_03
ORD IDord-12005e7f5b394d0f9d04a208106f351f
Source noteuspto-grants-2016_03