Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 86645970 | HCID 86645970 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86645973 | HCID 86645973 | 79% |
Reaction Steps
To a cooled mixture (0-5° C.) of (2R)-2-(4-{[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino}phenyl)propanoic acid (1 g, 3.16 mmol) in CH2Cl2 (20 mL), 1,1-carbonyldiimidazole (CDI) (0.512 g, 3.16 mmol) was added. After stirring for 1 h at 0-5° C. gaseous ammonia was bubbled into the mixture for 4 h and then left stirring at room temperature until the complete disappearance of the starting material. The reaction was quenched adding a H3PO4/H2PO4− buffer solution (pH=2.0, 5 ml), the two phases were separated and the organic one washed with the same buffer (3×10 mL) and water (3×10 mL), dried over anhydrous Na2SO4 and evaporated under vacuum to give (2R)-2-(4-{[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino}phenyl) propanamide (788 mg, 2.5 mmol) as a white solid (79%) used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08133911B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-aebfe6a14de546998dba0bcc4d26d2cc |
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| Source note | uspto-grants-2012_03 |
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