HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 10160216, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22140026 | HCID 22140026 | — |
| Reactant | HCID 86591756 | HCID 86591756 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10160216 | HCID 10160216 | — |
Reaction Steps
27 mg (0.09 mmol) of 3-(2-aminomethylphenyl)thiophene-2-carboxylic acid (3-methylbutyl)amide were dissolved in 3 ml of dry dichloromethane, and the solution was treated with 10 mg (0.1 mmol) of triethylamine and 24 mg (0.1 mmol) of benzyloxycarbonyloxysuccinimide. After a reaction time of 18 h, the mixture was diluted with 20 ml of dichloromethane, washed with saturated NaHCO3 solution and the organic phase was dried and concentrated. After purification by RP-HPLC, 27 mg (70%) of a colorless substance were obtained. MS (ES+): m/z=437 (M+1). 1H-NMR (CDCl3): δ=7.54-7.24 (10H, m), 6.90 (1H, d, J=4.8 Hz), 5.52 (1H, br s), 5.05 (3H, br s), 4.17 (2H, d, J=6.2 Hz), 3.16 (2H, m), 1.14 (1H, m), 1.07 (2H, q, J=7.0 Hz), 0.73 (6H, d, J=6.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06982279B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-2bfe4bde728a44c2acfe89fd1d1ce638 |
| Source note | uspto-grants-2006_01 |