HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexyl isothiocyanate → 2-Cyclohexylaminothiocarbonylthioethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexyl isothiocyanate | HCID 14289 | — |
| Reactant | N-triphenylmethylcysteamine | HCID 15616512 | — |
| Product | 2-Cyclohexylaminothiocarbonylthioethylamine | HCID 54230179 | — |
Reaction Steps
Cyclohexylisothiocyanate (0.2 ml) and N-triphenylmethylcysteamine (150 mg) were subjected to the reaction described in Reference 5. From the reaction product, triphenylmethyl was removed by the method described in Reference 4 to obtain 2-cyclohexylaminothiocarbonylthioethylamine (crude formate: 92 mg). The product was dissolved in anhydrous methanol (2 ml). Triethylamine (0.24 ml) and mitomycin A (97 mg: 0.8 molar equivalent) were added to the reaction solution which was then treated in a similar manner to that described in Example 1 to obtain Compound 37 (54 mg) in the form of grayish blue powders with a yield of 36%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863935 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-d9437d75619b443ba16c7a7f7b206621 |
| Source note | uspto-grants-1989_09 |