HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 5-Chloro-N-[1,3-dioxo-2-(4-piperidinylmethyl)-2,3-dihydro-1H-isoindol-4-yl]-2-thiophenecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 4-Piperidinemethanol | HCID 420771 | — |
| Reactant | 5-Chloro-N-(1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl)thiophene-2-carboxamide | HCID 4135740 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-N-[1,3-dioxo-2-(4-piperidinylmethyl)-2,3-dihydro-1H-isoindol-4-yl]-2-thiophenecarboxamide | HCID 12074892 | — |
Reaction Steps
At room temperature, 0.43 ml (2.73 mmol) of diethyl azodicarboxylate (DEAD) is added dropwise to a suspension of 670 mg (2.18 mmol) of 5-chloro-N-(1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl)-2-thiophenecarboxamide, 314 mg (2.73 mmol) of 4-hydroxymethylpiperidine and 716 mg (2.73 mmol) of triphenylphosphine in 8.7 ml of absolute THF. After 2 h at room temperature, the mixture is concentrated and the residue is separated by chromatography on silica gel (gradient: from dichloromethane/methanol 95:5 to dichloromethane/methanol/triethylamine 9:1:0.1). Yield: 430 mg (41.5% of theory); MS (ESI): m/z (%)=404 (M+H, 60), 145 (100); LC-MS (Method 4): rt (%)=3.02 (84).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189738B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-16cb1b4ae1754e45b11911f7cdd017be |
| Source note | uspto-grants-2007_03 |