HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → HCID 59367272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Benzyl N-(2-aminoethyl)carbamate | HCID 2794257 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59367272 | HCID 59367272 | 89.3% |
Reaction Steps
To a suspension of benzyl 2-aminoethylcarbamate LIX (3 g; 15.45 mmol) in anhydrous ethanol (20 mL) was added carbon disulfide (0.47 mL; 7.73 mmol). The mixture was heated under gently reflux for 22 h. After cooling to r.t., the product precipitated and was filtered, washed with anhydrous ethanol (3×) and air dried. Benzyl N-(2-{[(2-{[(benzyloxy)carbonyl]amino}ethyl)carbamothioyl]amino}ethyl)carbamate LX was obtained as white solid (2.97 g; 6.90 mmol; 89.3% yield). 1H NMR (DMSO-d6) 3.10-3.14 (m, 4H), 3.37-3.42 (m, 4H), 5.00 (s, 4H), 7.30-7.37 (m, 12H), 7.54 (brs, 2H); ESIMS found for C21H26N4O4S m/z 431.4 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08178490B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-0c897b4037a24c7cba3989e1a8142de4 |
| Source note | uspto-grants-2012_05 |