HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl isocyanate → 1-((S)-1-{2-[4-(4-CHLORO-PHENYL)-PIPERAZIN-1-YL]-5-OXO-6,7-DIHYDRO-5H-5lambda4-THIENO[3,2-D]PYRIMIDIN-4-YL}-PYRROLIDIN-2-YLMETHYL)-3-PHENYLUREA
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | HCID 66735925 | HCID 66735925 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-((S)-1-{2-[4-(4-CHLORO-PHENYL)-PIPERAZIN-1-YL]-5-OXO-6,7-DIHYDRO-5H-5lambda4-THIENO[3,2-D]PYRIMIDIN-4-YL}-PYRROLIDIN-2-YLMETHYL)-3-PHENYLUREA | HCID 59708430 | — |
Reaction Steps
100 mg C—((S)-1-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-5-oxo-6,7-dihydro-5H-5λ4-thieno[3,2-d]pyrimidin-4-yl}-pyrrolidin-2-yl)-methylamine trifluoroacetate, Diastereomer 2 (Example 226) (see scheme 3, 3.17.2) are placed in 2 ml dichloromethane and 30 μl phenylisocyanate are added. The reaction mixture is stirred for 4 hours at ambient temperature and then evaporated to dryness. The product is purified by preparative HPLC (method A). 64 mg of the product are obtained as a powder. Analytical HPLC-MS (method D): RT=1.33 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822474B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-6deefbb6c5af4b72b8cb1fb4d0502200 |
| Source note | uspto-grants-2014_09 |