HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(2-Amino-4-chloro-6-methyl-pyrimidin-5-ylethynyl)-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | m-Ethynylphenol | HCID 139144 | — |
| Reactant | 4-Chloro-5-iodo-6-methylpyrimidin-2-amine | HCID 11644720 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2-Amino-4-chloro-6-methyl-pyrimidin-5-ylethynyl)-phenol | HCID 58513344 | — |
Reaction Steps
The title compound is synthesized according to general procedure GP2 starting from 1.5 g (5.7 mmol) 4-chloro-5-iodo-6-methyl-pyrimidin-2-ylamine (GP3) and 986 mg (8.4 mmol) 3-ethynyl-phenol using 106 mg (0.56 mmol) CuI, 390 mg (0.56 mmol) PdCl2(PPh3)2 and 8 mL (55 mmol) triethylamine in 12 mL dry DMF. For the work-up the solvent is removed in vacuo and the product is purified by chromatography on silica gel (DCM/MeOH gradient) and subsequently RP-HPLC (ACN/H2O gradient). Yield: 419 mg (29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916548B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-8f5f174b38794f44901ed39c5f7f576e |
| Source note | uspto-grants-2014_12 |