HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542952Generated: October 25, 2026
N,N-Dimethylaniline → 2,4-Diamino-5-(4-amino-3,5-dimethoxy-benzyl)-6-chloropyrimidine
https://huagongshe.com/reaction/542952
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2,6-diamino-5-[(4-amino-3,5-dimethoxyphenyl)methyl]-1H-pyrimidin-4-one | HCID 178488798 | — |
| Product | 2,4-Diamino-5-(4-amino-3,5-dimethoxy-benzyl)-6-chloropyrimidine | HCID 21280993 | — |
Reaction Steps
2.5 G. of dimethylaniline were added dropwise to a suspension of 2.9 g. of 2,6-diamino-5-(4-amino-3,5-dimethoxy-benzyl)-4-pyrimidinol in 15 ml. of phosphorus oxychloride with stirring. The mixture was brought to boil in 1 hour and then boiled under reflux for 4 hours. Thereafter, 8 to 9 ml. of phosphorus oxychloride were removed by distillation under reduced pressure and the residue was poured on to 80 g. of ice with stirring. The mixture was left to stand at room temperature for 6 days and then 35 ml. of concentrated ammonia were added portionwise. After standing for 2 hours, the solid material was removed by filtration under vacuum, dried, recrystallized from dimethylformamide/ether, whereby there was obtained 2,4-diamino-5-(4-amino-3,5-dimethoxy-benzyl)-6-chloro-pyrimidine having a melting point of 222°-224° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04659818 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-435cd14ddd554056a950b40a7e4d5b8b |
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| Source note | uspto-grants-1987_04 |
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