HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-phenylbutan-2-one → 2-Amino-6-phenethyl-3,7-dihydropyrrolo[2,3-d]pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-phenylbutan-2-one | HCID 10921160 | — |
| Reactant | 2-Aminoisocytosine | HCID 135408763 | — |
| Product | 2-Amino-6-phenethyl-3,7-dihydropyrrolo[2,3-d]pyrimidin-4-one | HCID 135479891 | 39% |
Reaction Steps
FIG. 19 presents the method used to synthesize 2-amino-6-phenethyl-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one 9. Phenylpropanoyl chloride7 was reacted with CH2N2 in the presence of gaseous hydrogen chloride and ether to produce 1-chloro-4-phenyl-2-butanone 8. 1-chloro-4-phenyl-2-butanone 8 was reacted with 2,6-diamino-3H-pyrimidin-4-one 1 to produce 2-amino-6-phenethyl-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one 9 at a 39% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562969B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-6d4d9d7c49004208bdb0460f4f9d7e6f |
| Source note | uspto-grants-2003_05 |