Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| Reactant | (4-Chlorophenoxy)acetic acid | HCID 26229 | — |
| Reactant | Cyclohexyl isocyanide | HCID 79129 | — |
| Reactant | tert-Butyl (2-amino-4-chloro-5-fluorophenyl)carbamate | HCID 67375046 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 42606856 | HCID 42606856 | 37% |
Reaction Steps
To a solution of (2-amino-4-chloro-5-fluoro-phenyl)-carbamic acid tert-butyl ester (26.07 mg, 0.10 mmol, 1.0 equiv; Intermediate D) in MeOH (1.0 mL) was added cyclohexanecarbaldehyde (16.83 mg, 18.05 1, 0.15 mmol, 1.5 equiv; [2043-61-0]) and the mixture stirred at rt. After 30 min, (4-chloro-phenoxy)-acetic acid (18.66 mg, 0.10 mmol, 1.0 equiv; [CAS RN 122-88-3]) and cyclohexyl isocyanide (10.92 mg, 12.27 1, 0.10 mmol, 1.0 equiv; [931-53-3]) were added and stirring continued at rt for 2 h. A solution of 4 M HCl in dioxane (0.2 mL) was added and the reaction mixture stirred at rt overnight. Removal of the solvent mixture under reduced pressure and purification by preparative HPLC on reversed phase eluting with a gradient of acetonitrile/water provided 19.6 mg (37%) of the title compound. MS (ISP): 532.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790904B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-5b5bdbce63a344b7806fa7357f5b568f |
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| Source note | uspto-grants-2010_09 |
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