Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86649532 | HCID 86649532 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58092783 | HCID 58092783 | — |
Reaction Steps
N-(7-Cyclopropylmethyl-4,5-dihydro-benzo[1,2-d;3,4-d′]bisthiazol-2-yl)-acetamide (Stage V.2, 180 mg, 0.589 mmol) was dissolved in EtOH (10 mL) and 36% HCl (1.193 g, 11.79 mmol) added. The RM was heated to 90° C. for 16 h then cooled and extracted with EtOAc/H2O. The organic layer was dried over Na2SO4 and evaporated. The crude material was chromatographed with MPLC C18 H2O 0.1% TFA/CH3CN 0.1% TFA, gradient 0-50%. Product containing fractions were neutralized with NaHCO3, extracted with EtOAc and lyophilized from dioxane to give the title compound (M+H=264.2; M−H=262.1; tR 4.183 min (Method F)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357707B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-125ed3a044e441eaafcc8dc2139344b7 |
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| Source note | uspto-grants-2013_01 |
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