HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876152Generated: October 30, 2026
Sodium Cyanide → 4-[(4-Methoxyphenyl)(methyl)amino]quinazoline-2-carbonitrile
https://huagongshe.com/reaction/1876152
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | (2-Chloroquinazolin-4-yl)-(4-methoxyphenyl)-methylamine hydrochloride | HCID 86639964 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[(4-Methoxyphenyl)(methyl)amino]quinazoline-2-carbonitrile | HCID 57516547 | 139.4% |
Reaction Steps
To a solution of (2-chloroquinazolin-4-yl)-(4-methoxyphenyl)-methylamine hydrochloride (56 mg, 0.17 mmol) in 1 mL of DMSO and 0.5 mL of 2-propanol were added sodium cyanide (16 mg, 0.34 mmol) and 1,4-diazabicyclo[2.2.2]octane (9 mg, 0.084 mmol). The mixture was heated at 35° C. for 1 d with stirring. The solution was diluted with 5 mL of water and 10 mL of ethyl acetate. The organic layer was washed with water, then dried and concentrated. The resulting crude material was purified by silica gel column chromatography to give the title compound (34 mg, 70%). 1H NMR (CDCl3, 400 MHz) δ 7.85 (d, 1H, J=8.4 Hz), 7.64 (t, 1H, J=6.8 Hz), 7.14 (m, 3H), 6.96 (m, 3H), 3.86 (s, 3H), 3.61 (s, 3H); ESI-MS m/z 291 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309562B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-bfb59ba6a15e49e489559cf83a4456ce |
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| Source note | uspto-grants-2012_11 |
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