Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 57542085 | HCID 57542085 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 11656082 | HCID 11656082 | 20.6% |
Reaction Steps
A solution of methyl [7-Chloro-5-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)imidazo[1,2-c]-pyrimidin-8-yl]acetate (0.100 g, 0.199 mmol) in dioxane (1.00 mL) was added 6N HCl aq. (0.5 mL) and heated to 100° C. for 22 hours. After cooling to room temperature, the volatiles was removed under reduced pressure to generate a precipitate which was suspended in water, collected by suction, rinsed with water and diethyl ether, and dried under high vacuum to give [7-chloro-5-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)imidazo[1,2-c]pyrimidin-8-yl]acetic acid as a white powder (0.020 g, 20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750014B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-37c20b9be7a04b77af1a3e9e1ee1e5bb |
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| Source note | uspto-grants-2010_07 |
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