HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 68772556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Methyl 6-aminohexanoate | HCID 1810164 | — |
| Reactant | HCID 68424066 | HCID 68424066 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68772556 | HCID 68772556 | 52% |
Reaction Steps
To a suspension of 3-(1E)-(4-(2-(4-fluorophenyl)-3-(cyclopropylamino)-3-oxoprop-1-en-1-yl)phenyl)acrylic acid (prepared according to the procedure described in Example 59, step-I) (0.35 g, 1 mmol) in DMF (15 mL) EDCI (0.83 g, 2 mmol), HOBt (0.13 g, 1 mmol), methyl 6-aminocaproate (0.16 g, 0.9 mmol), were added, followed by triethylamine (0.4 mL, 3 mmol). The reaction mixture was stirred for 2 hours after which the mixture was added to cold water (50 mL). The aqueous layer was extracted with ethyl organic layer was dried over anhydrous Na2SO4 and concentrated to get the crude compound. The crude yellow colored compound was washed with ethyl acetate/hexane (0.5/9.5, 2×20 mL) to afford the title compound as a yellow solid (0.25 g, 52% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450525B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-fc79db691d0c476bbbd8dc50de5dc3a6 |
| Source note | uspto-grants-2013_05 |