Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2,2,4,4,6,6,8,8-Octachloro-2lambda5,4lambda5,6lambda5,8lambda5-1,3,5,7,2,4,6,8-tetrazatetraphosphocine | HCID 76285 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 136408031 | HCID 136408031 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86715518 | HCID 86715518 | 16.2% |
Reaction Steps
6-(2-(3-Chloro-4-fluorophenyl)pyridin-3-yl)pyrido[3,2-d]pyrimidin-4 (3H)-one (100 mg, 0.28 mmol), phosphonitrilic chloride (100 mg, 0.28 mmol) and as stir bar were transferred to a vial, capped and placed under nitrogen atmosphere. Dry acetonitrile (3 mL) was transferred and allowed the contents to stir at room temperature. i-Pr2NEt was added for 2 min to the heterogeneous slurry. Upon stirring the red homogeneous slurry for 2 h, nitrogen balloon was replaced with NH3 balloon and stirred. After stirring the contents for 6 h, the reaction mixture was concentrated and the crude residue was partitioned between chloroform/water. Organic layer was removed and re-extracted the aqueous layer with chloroform. Usual workup and purification by preparative HPLC provided 6-(2-(3-Chloro-4-fluorophenyl)pyridin-3-yl)pyrido[3,2-d]pyrimidin-4-amine (16 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145433B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-ce1dde7a64314c59919b6e9665bbdbb3 |
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| Source note | uspto-grants-2015_09 |
|---|