HuagongsheHuagongshe Chemistry Print Report · For research reference only
5,6-Dimethoxyindoline → 5,6-dimethoxy-1-(2-(4-nitro-1H-pyrazol-1-yl)ethyl)indoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5,6-Dimethoxyindoline | HCID 11062978 | — |
| Reactant | (4-nitro-1H-pyrazol-1-yl)acetaldehyde | HCID 25220516 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5,6-dimethoxy-1-(2-(4-nitro-1H-pyrazol-1-yl)ethyl)indoline | HCID 68283452 | — |
Reaction Steps
To a solution of 2-(4-nitro-1H-pyrazol-1-yl)acetaldehyde (942 mg, 6.08 mmol) in DCM (60.0 mL), 5,6-dimethoxyindoline (from step 1) (1.09 g, 6.08 mmol) and STAB (1.55 g, 7.29 mmol) was added. After stirring at rt for 1 h, the reaction mixture was quenched with water and extracted with DCM (2×). The combined org. layers were concentrated and purification was performed by FC (EtOAc/hex 1:4 to 1:1) to yield 5,6-dimethoxy-1-(2-(4-nitro-1H-pyrazol-1-yl)ethyl)indoline as a brown solid. LC-MS conditions B: tR=0.65 min, [M+H]+=319.19.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09303023B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-5c6c99cad5264a77b733aa7509b4e614 |
| Source note | uspto-grants-2016_04 |