Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | [2-(5-Acetyl-thiophen-2-ylmethyl)-thiazol-4-yl]-carbamic acid tert-butyl ester | HCID 67128627 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67128443 | HCID 67128443 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of [2-(5-acetyl-thiophen-2-ylmethyl)-thiazol-4-yl]-carbamic acid tert-butyl ester (75 mg, 0.22 mmol) in dry CH2Cl2 (2.2 mL) was treated at 0° C. with HCl (0.55 mL of a 4M solution in dioxane, 2.22 mmol). After stirring at 0° C. for 1 h, the reaction mixture was stirred at rt for 16 h. The solvents were removed under reduced pressure to give the title compound as a light brown solid. LC-MS-conditions 02: tR=0.71 min, [M+AcCN+H]+=280.14.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674111B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-74fc325af6d84421b9debea7fdfb52c5 |
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| Source note | uspto-grants-2014_03 |
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