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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 136636244 | HCID 136636244 | — |
| Catalyst | Cobalt(II) chloride hydrate | HCID 16211468 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-(aminomethyl)-2-phenylquinazolin-4(3H)-one | HCID 136636245 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278910B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-12005e7f5b394d0f9d04a208106f351f |
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| Source note | uspto-grants-2016_03 |
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