HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 86612297, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 2-(2-bromophenyl)acetate | HCID 2780092 | — |
| Reactant | HCID 11695413 | HCID 11695413 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86612297 | HCID 86612297 | — |
Reaction Steps
Stir a solution of N-((1R,3S)-5-methoxy-6-methyl-3-(4-piperidinyl)-1-isochromanyl-methyl)formamide (200 mg, 0.58 mmole), ethyl 2-bromophenylacetate (229 mg, 0.94 mmole) and diisopropylethylamine (243 mg, 1.88 mmole) in acetonitrile overnight at room temperature. Add ethyl acetate and water (2 mL each), then separate the organic phase and dry over Na2SO4. Purify the crude product on a 4 g silica gel column (eluting with ethyl acetate:heptane 3:1). Collect the appropriate fractions and concentrate to obtain the title compound. It was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919508B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-91279cedad6b4d69ac7ee744a0ad91f7 |
| Source note | uspto-grants-2011_04 |