HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → N-(2-Amino-1,3-benzothiazol-6-yl)thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-[(2-Amino-1,3-benzothiazol-6-yl)carbamothioyl]benzamide | HCID 21878462 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-Amino-1,3-benzothiazol-6-yl)thiourea | HCID 21878483 | 66.5% |
Reaction Steps
A suspension of 1-(2-amino-benzothiazol-6-yl)-3-benzoyl-thiourea (Example 2, 0.2 g, 0.61 mmol) and 2.0 N NaOH (0.67 mL, 1.34 mmol) in 10 mL of THF was heated at reflux for 4 hours. Upon cooling, a yellow solid precipitated which was filtered. Yield: 66.5%, 1H-NMR (DMSO-d6): δ 9.55 (s, 1H); 7.64 (d, 1H, J=1.8 Hz); 7.44 (s, 2H); 7.27 (m, 2H); 7.03 (dd, 1H, J=8.0, 2.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07141595B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-bc8317bcceff476ca61e19a38b1a2481 |
| Source note | uspto-grants-2006_11 |