Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86626617 | HCID 86626617 | — |
| Reactant | HCID 178514161 | HCID 178514161 | — |
| Product | HCID 86626618 | HCID 86626618 | — |
Reaction Steps
N-(4-hydrazino-4-oxobutyl)thiourea (128.50 mg; 0.73 mmol; 1.00 eq.) is dissolved in MeOH (7.00 ml) and triethylamine (0.30 ml; 2.19 mmol; 3.00 eq.). The solution is cooled down to 0° C. and intermediate 1 (201.20 mg; 0.73 mmol; 1.00 eq.) is added as a solid. The mixture is stirred 2 hours at RT. Solvents are evaporated and N-{2-[(4-hydrazino-4-oxobutyl)amino]-4′-methyl-4,5′-bi-1,3-thiazol-2′-yl}acetamide is used in the next step without further purification. M− (ESI): 353; M+ (ESI): 355. HPLC, Rt: 1.19 min (purity: 95.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09150561B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-7b6b101866694cfebc93e979ffc6dd2c |
|---|
| Source note | uspto-grants-2015_10 |
|---|