HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentyl isothiocyanate → 4-[2-(Cyclopentylamino)-1,3-thiazol-4-yl]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentyl isothiocyanate | HCID 141792 | — |
| Reactant | Cyclopentylthiourea | HCID 736945 | — |
| Reactant | 4-(2-bromoacetyl)benzoic Acid | HCID 2756836 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[2-(Cyclopentylamino)-1,3-thiazol-4-yl]benzoic acid | HCID 59807296 | — |
Reaction Steps
Isothiocyanato-cyclopentane (4 g) in ammonia (37% in water, 8 mL) and methanol (32 mL) was stirred for 16 hours, filtered of and dried. The Cyclopentyl-thiourea (2.06 mmol) and 4-(2-Bromo-acetyl)-benzoic acid (2.06 mmol) were mixed in THF (12 mL). After stirring at room temperature for 5 minutes the mixture was heated to 80° C. for 2 hours. The mixture was then cooled to room temperature and filtered. The solid was washed with a small amount of diethylether and dried. m/z=289.05 in MS ES+, which was characterized by hplc and MS and used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915300B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-646b3ae29c9346a8bf3197e800676313 |
| Source note | uspto-grants-2011_03 |