Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-(2-Aminopropyl)benzyl alcohol | HCID 24721512 | — |
| Reactant | HCID 57593119 | HCID 57593119 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 57593127 | HCID 57593127 | — |
Reaction Steps
A mixture of [3-(2-amino-propyl) -phenyl]-methanol (300 mg, 1.8 mmol) and 2-(2-methanesulfinyl-pyrimidin-4-ylamino) -3-methyl-6-phenyl-3H-pyrimidin-4-one (300 mg, 0.9 mmol) in NMP (8 mL) was heated to 100° C. for 16 h. The reaction was cooled to room temperature and EtOAc was added. The mixture was then washed with H2O three times, brine once, dried (MgSO4), filtered, concentrated under vacuum, and purified by preparative-scale TLC to give the product. M+1: 443.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07504403B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-c36ac95a2c8f4a28bbcb4b4b9223578e |
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| Source note | uspto-grants-2009_03 |
|---|