HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 70675028, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 2-Aminoadamantane hydrochloride | HCID 25331 | — |
| Reactant | HCID 70683867 | HCID 70683867 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70675028 | HCID 70675028 | 54% |
Reaction Steps
To 2-(1,1-dioxido-6-phenyl-1,2,6-thiadiazinan-2-yl)acetic acid (100 mg, 0.37 mmol) in DCM (5 mL), were added 2-adamantan amine HCl (105 mg, 0.56 mmol), TEA (74.9 mg, 0.74 mmol) and EDCI (212.8 mg, 1.11 mmol). The reaction mixture was agitated for 5 hr at room temperature and extracted using CH2Cl2 and brine. The organic layer was dried over MgSO4. The residue was purified by silica gel column chromatography to give N-(adamantan-2-yl)-(1,1-dioxido-6-phenyl-1,2,6-thiadiazinan-2-yl)acetamide (80 mg, 54%). 1H NMR (300 MHz, CDCl3): δ 7.41-7.26 (m, 5H), 7.02-6.99 (brd, 1H), 4.07 (m, 1H), 3.94 (s, 2H), 3.81-3.74 (m, 4H), 2.03-1.94 (m, 4H), 1.85-1.74 (m, 10H), 1.66-1.60 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073906B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-2ab16c5eacc2484fa8968118a634ea60 |
| Source note | uspto-grants-2015_07 |