HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381001Generated: November 1, 2026
Formaldehyde → (4-Dimethylamino-phenyl)-(2-methyl-quinazolin-4-yl)-methyl-amine
https://huagongshe.com/reaction/2381001
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine | HCID 11311597 | — |
| Solvent | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Product | (4-Dimethylamino-phenyl)-(2-methyl-quinazolin-4-yl)-methyl-amine | HCID 11403596 | 80% |
Reaction Steps
To a solution of (2-methyl-quinazolin-4-yl)-(4-amino-phenyl)-methylamine (14 mg, mmol) in 1.5 mL of 37% aqoues formaldehyde solution and 10 uL of glacial acetic was added Sodium cyanoborohydride (15 mg, 0.24 mmol) and the mixture was stirred at room temperature for 2 h. The reaction mixture was quenched by adding 50 uL of 1N HCl. It was diluted with 50 mL of ethyl acetate, washed with saturated sodium bicarbonate, and followed by saturated sodium chloride. The organic layer was dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified by column chromatography (25% ethyl acetate/hexanes) on silica gel to give the title compound (12.4 mg, 0.042 mmol, 80%). 1H NMR (CDCl3): 7.71 (m, 1H), 7.50 (ddd, J=8.4, 6.9, 1.5, 1H), 7.03-7.09 (m, 3H), 6.95 (ddd, J=8.1, 6.6, 0.9, 1H), 6.70 (m, 2H), 3.57 (s, 3H), 2.99 (s, 6H), 2.71 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258145B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-6c85d54bde724d3e809b69a34e7fa343 |
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| Source note | uspto-grants-2012_09 |
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