HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623205Generated: October 29, 2026
Ammonia → Pyrimidine, 1,4,5,6-tetrahydro-2-methyl-5-phenyl-, monohydrochloride
https://huagongshe.com/reaction/623205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | 78533-94-5 | HCID 21290602 | — |
| Product | Pyrimidine, 1,4,5,6-tetrahydro-2-methyl-5-phenyl-, monohydrochloride | HCID 217092 | 32% |
Reaction Steps
A mixture consisting of 20 g (0.0897 mol) of 2-phenylpropane-1,3-diamine dihydrochloride, 10.76 g (0.269 mol) of sodium hydroxide pellets and 8.48 g (0.0897 mol) of acetamidine hydrochloride is heated under reflux until the evolution of NH3 has ended. The reaction medium is cooled, the insoluble material is filtered off and discarded, the filtrate is acidified with ethanol containing HCl and evaporated to half the volume, and the insoluble material formed is filtered off. The filtrate is diluted with an equal volume of ether, the insoluble material formed is filtered off and the resulting filtrate is evaporated to dryness. Recrystallization of the evaporation residue from an acetone/ethanol mixture (1:1 v/v) gives 6 g (yield: 32%) of CRL 41 352. M.p. (inst.)=220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04774248 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-8f9194ded88f4a0fa00799c8ab753fbf |
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| Source note | uspto-grants-1988_09 |
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