HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetamide → Deoxy modafinil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetamide | HCID 6580 | — |
| Reactant | Benzhydryl thiuronium bromide | HCID 22066263 | — |
| Product | Deoxy modafinil | HCID 9965017 | — |
Reaction Steps
In Steps 2 and 3, the S-benzhydrylthiouronium bromide formed in step 1 is converted to the corresponding thiol, and then reacted with chloroacetamide to form 2-(benzhydrylthiyl)acetamide. For example, the thiourea can be converted to the thiol by reaction with a suitable base. The reaction steps 2 and 3 can be carried out in the same reaction vessel as was employed in step 1, without isolation of any intermediates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07057069B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-6f51193a1bec450cac8eecea6f36b408 |
| Source note | uspto-grants-2006_06 |