Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 2,6-Difluorophenyl isothiocyanate | HCID 4031601 | — |
| Reactant | HCID 178508036 | HCID 178508036 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178521598 | HCID 178521598 | 46% |
Reaction Steps
4-{[5-Amino-4-(cyclopentylamino)pyrimidin-2-yl]amino}trans-cyclohexan-1-ol (1.13 mmol, 330 mg) was dissolved in DMF (8.5 mL) and 2,6-difluorophenylisothiocyanate (1.13 mmol, 0.146 mL) was added. The reaction mixture was stirred at room temperature for about 90 minutes. Ethanol (2.5 mL) was added and the reaction mixture was stirred for about an additional 30 minutes. N,N-Diisopropylcarbodiimide (3.40 mmol, 0.532 mL) was added and the reaction mixture was stirred overnight. Solvent was removed and the residue was purified using column chromatography (SiO2, 1:1 n-hexanes/ethyl acetate→ethyl acetate→1% methanol/ethyl acetate) to give the desired product (222.5 mg, 46% yield). ES-MS: 429 (M+1). Tetrahydrofuran can also be used as solvent in this step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723340B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-4eeb929036724a9d8b4db68116762de1 |
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| Source note | uspto-grants-2010_05 |
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