HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 5-((Benzyloxy)methyl)-2-butyl-7-(3-(4-ethylpiperazin-1-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-((Benzyloxy)methyl)-2-butyl-7-(3-(piperazin-1-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine | HCID 118453784 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dimethyl sulfoxide methanol | HCID 22036561 | — |
| Product | 5-((Benzyloxy)methyl)-2-butyl-7-(3-(4-ethylpiperazin-1-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine | HCID 118453813 | 69.1% |
Reaction Steps
To a solution of 5-((benzyloxy)methyl)-2-butyl-7-(3-(piperazin-1-yl)prop-1-yn-1-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine (38 mg, 0.088 mmol) in anhydrous N,N-dimethylformamide (1 mL) at room temperature was added triethylamine (25 μL, 0.179 mmol) and iodoethane (10 μL, 0.125 mmol). The reaction was stirred at room temperature for 5 hours. The reaction was evaporated in vacuo to yield a pale yellow oil. The oil was dissolved in MeOH:DMSO (1:1) (1 mL) and purified by MDAP (Method B). The appropriate fraction was evaporated in vacuo to yield the title compound as a pale yellow oil (28 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428512B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-23d2dabc017d4546a73b03b468adb457 |
| Source note | uspto-grants-2016_08 |