Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 67194218 | HCID 67194218 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67194659 | HCID 67194659 | 80% |
Reaction Steps
To a stirred solution of (R)-2-((tert-butoxycarbonyl)(4-(5-(3-cyano-4-isopropoxyphenyl)-1,3,4-thiadiazol-2-yl)-2,3-dihydro-1H-inden-1-yl)amino)acetic acid (20 mg, 0.03) mmol in 1,4-dioxane (0.5 mL) was added 4N HCl in 1,4-dioxane (0.2 mL). The mixture was stirred at 50° C. for 2 h before it was concentrated and triturated with ether to afford 13 mg of (R)-2-((4-(5-(3-cyano-4-isopropoxyphenyl)-1,3,4-thiadiazol-2-yl)-2,3-dihydro-1H-inden-1-yl)amino)acetic acid as yellow-green solid. LCMS-ESI (m/z) calculated for C23H22N4O3S: 434.14, found 435.2 [M+H]+, tR=2.51 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507538B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-88f52541c51a44e686f81a85406d26ed |
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| Source note | uspto-grants-2013_08 |
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