HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloropyrimidine → 3-(2-Methyl-pyrimidin-5-yl)-10-(pyrimidin-2-ylamino)-decanoic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 10-Amino-3-(2-methyl-pyrimidin-5-yl)-decanoic acid ethyl ester | HCID 20622483 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(2-Methyl-pyrimidin-5-yl)-10-(pyrimidin-2-ylamino)-decanoic acid ethyl ester | HCID 20622484 | 66.5% |
| Product | NH4OEt | HCID 22341770 | 1% |
Reaction Steps
A solution of 24-7 (360 mg, 1.17 mmol), 2-chloropyrimidine (145 mg, 1.26 mmol), and N,N-diisopropylethylamine (456 mg, 3.53 mmol) in ethanol (5 mL) was heated to 65° C. in a sealed tube (4 days). The solvent was removed in vacuo and the residue diluted in aqueous sodium carbonate and extracted with two portions of dichloromethane. The combined organics were washed with brine and dried (Na2SO4). The solvent was removed in vacuo. PCTLC (SiO2, 4 mm, 1% NH4OEt; 10% EtOH; 90% CH2Cl2) afforded 24-8 (150 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153862B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-edfcac586d7f487986c14474eadd2a0e |
| Source note | uspto-grants-2006_12 |