HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Ethoxyacryloyl chloride → HCID 136052910, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Ethoxyacryloyl chloride | HCID 5325500 | — |
| Reactant | 5-[(4-Aminophenyl)methyl]-1-methyl-3-propyl-1,4-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one | HCID 135815262 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 136052910 | HCID 136052910 | — |
Reaction Steps
(E)-3-ethoxyacryloyl chloride (J. Chem. Soc; 1958,153) (298 mg, 0.0022 mol), was added dropwise to an ice-cooled solution of 5-(4-aminobenzyl)-1-methyl-3-propyl-6,7-dihydro-1H-pyrazolo[4,3-d]pyrimidin-7-one (600 mg, 0.002 mol) in pyridine (15 ml) and the reaction stirred at room temperature for 20 hours. The mixture was partitioned between water (30 ml) and dichloromethane (30 ml), the aqueous layer acidified to pH1 with 2M aqueous hydrochloric acid solution and then extracted with dichloromethane (2×40 ml). The combined organic extracts were dried (MgSO4), filtered and evaporated under reduced pressure, to give, after recrystallisation from ethyl acetate/methanol the title compound (483 mg), m.p.241-243° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235742B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-920344beb9654c0b8b85369e03ce3b9a |
| Source note | uspto-grants-2001_05 |