HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → 5-Chloro-7-(4-methoxypent-1-yn-1-yl)-1,3-benzodioxol-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 5-Chloro-7-iodo-1,3-benzodioxol-4-amine | HCID 17980527 | — |
| Reactant | 4-Methoxypent-1-yne | HCID 86601564 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Chloro-7-(4-methoxypent-1-yn-1-yl)-1,3-benzodioxol-4-amine | HCID 68881217 | 92% |
Reaction Steps
5-chloro-7-iodo-1,3-benzodioxol-4-amine (600 mg, 2.02 mmol) and 4-methoxypent-1-yne (500 mg, 5.10 mmol) in ethyl acetate (8 ml) were cooled in ice-methanol, under an atmosphere of nitrogen, then treated with bis(triphenylphosphine)palladium(II) dichloride (141 mg, 10 mol %) followed by copper(I) iodide (38 mg, 10 mol %) and diisopropylamine (407 mg, 5.69 mmol). The reaction was allowed to warn to room temperature and stirred 90 min then filtered through Celite. The filtrate was purified by column chromatography on silica using a 1:1 mixture of methyl tert-butyl ether and iso-hexane as eluent to give 5-chloro-7-(4-methoxypent-1-yn-1-yl)-1,3-benzodioxol-4-amine (495 mg, 92%) as a dark brown oil;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504408B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-64136a8cd324442f9a988bcc15cbb60e |
| Source note | uspto-grants-2009_03 |