Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 68767233 | HCID 68767233 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68764955 | HCID 68764955 | — |
Reaction Steps
A mixture of 1.05 g of methyl 5-[6-({[tert-butyl(dimethyl)silyl]oxy}methyl)-3H-imidazo[4,5-c]pyridin-3-yl]-3-{[2-(trifluoromethyl)benzyl]oxy}thiophene-2-carboxylate (compound B2a) and 100 ml of a saturated solution of ammonia in methanol was stirred in an autoclave at 120° C. for 3.5 h. The reaction mixture was allowed to cool down to room temperature, concentrated to dryness, dissolved in dichloromethane and filtered through a plug of silica gel (eluents: dichloromethane/ethyl acetate) to yield the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273890B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-4d6d2021265e4503bf5f34c9659f491a |
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| Source note | uspto-grants-2012_09 |
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