Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Serinol | HCID 68294 | — |
| Reactant | HCID 23155131 | HCID 23155131 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59725991 | HCID 59725991 | 60.3% |
Reaction Steps
In dichloromethane (3.5 mL), 60 mg (0.105 mmol) of 3-(3-{4-[6-(tert-butoxycarbonyl-methylamino)-purin-9-yl]phenyl}ureido)-5-(trifluoromethyl)benzoic acid was dissolved, and 54.9 μL (0.63 mmol) of oxalyl chloride was slowly added thereto and the mixture solution was stirred under refluxing for 1.5 hours. The solvent was distilled under reduced pressure from the reaction solution and the obtained residue was dissolved in tetrahydrofuran (0.75 mL). The tetrahydrofuran solution thus prepared was added dropwise to a methanol (0.5 mL)/tetrahydrofuran (0.25 mL) solution of 28.7 mg (0.315 mmol) of 2-amino-1,3-propanediol and the resulting solution was stirred at room temperature for 1.5 hours. The solvent was distilled under reduced pressure from the reaction solution and the obtained residue was purified by silica gel column chromatography (dichloromethane:methanol=20:1 to 5:1) to obtain 40.8 mg (60%) of a target product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609656B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-d0c66fa5a5f94ac5a362286c77fe57b3 |
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| Source note | uspto-grants-2013_12 |
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