HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903838Generated: October 25, 2026
Guanidine → 2,4-Diamino-5-(4-methoxy-1-naphthylmethyl)pyrimidine hydrochloride
https://huagongshe.com/reaction/1903838
Participants
| Role | Name | HCID | Charge |
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| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3-Anilino-2-(4-methoxy--naphthylmethyl)acrylonitrile | HCID 70451880 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 2,4-Diamino-5-(4-methoxy-1-naphthylmethyl)pyrimidine hydrochloride | HCID 23310604 | — |
Reaction Steps
To 65 mL of ethanolic guanidine solution prepared from 3.42 g (35.8 mmol) of guanidine hydrochloride and 2.00 g (37.0 mmol) of sodium methoxide was added 9.00 g (28.6 mmol) of 3-anilino-2-(4-methoxy-1-naphthylmethyl)acrylonitrile. The solution was heated under reflux for 1.5 hr, and then 60 mL of 2-methoxyethanol was added. The internal temperature was allowed to gradually increase to 108° by distillation of the ethanol, after which it was heated at this temperature for 2.5 hr. The hot mixture was filtered, and the precipitate (7.04 g, 87% of crude product) recrystallized from 30% ethanol in the presence of hydrochloric acid, to give the title compound; mp 312°-314° dec. Anal. Calcd for C16H16N4O.HCl: C, 60.66; H, 5.41; N, 17.69; Cl, 11.19. Found: C, 60.67; H, 5.45; N, 17.70; Cl, 11.19.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04438267 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-e9e75cf762184ffc868aed76262fc2ec |
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| Source note | uspto-grants-1984_03 |
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