HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 67267117, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 56953891 | HCID 56953891 | — |
| Reactant | HCID 86607170 | HCID 86607170 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67267117 | HCID 67267117 | 77.8% |
Reaction Steps
A solution of (4-amino-2-methylphenyl)-carbamic acid propyl ester (21 mg, 0.10 mmol) and 5-dimethylamino-3-methyl-benzo[b]thiophene-2-carbaldehyde (26 mg, 0.12 mmol) in acetonitrile (0.5 mL) was heated at 170° C. for 2 minutes using a Personal Chemistry Smith Synthesizer microwave device. After cooling to room temperature, a solution of sodium cyanoborohydride (25 mg, 0.40 mmol) in methanol (0.1 mL) was added followed by acetic acid (50 μL), and the mixture was stirred for 30 minutes. It was partitioned between saturated aqueous sodium bicarbonate (10 mL) and ethyl acetate (10 mL), and the organic layer was dried over sodium sulfate and evaporated. Preparative LC-MS afforded the title compound (32 mg, 77% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07906537B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-408200737f2c4dec9f8c976d07b8de5a |
| Source note | uspto-grants-2011_03 |