Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 70557870 | HCID 70557870 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68176356 | HCID 68176356 | — |
Reaction Steps
To a solution of 4-((4-chloro-benzyl)-{1-[2-(3,5-dimethyl-phenyl)-acetyl]-2-methyl-azetidine-2-carbonyl}-amino)-butyric acid ethyl ester, Intermediate 146 (1 eq.) in MeOH was added an aqueous solution of NH3 (20% in water). The reaction was stirred at 60° C. for 15 h then cooled to 20° C. The solvents were evaporated under reduced pressure and the crude was purified by preparative LCMS to afford 1-[2-(3,5-dimethyl-phenyl)-acetyl]-2-methyl-azetidine-2-carboxylic acid (3-carbamoyl-propyl)-(4-chloro-benzyl)-amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759334B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-a0011fec58704b86bbada38f15014002 |
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| Source note | uspto-grants-2014_06 |
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