HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1-(4-(3-(Cyclopropylmethyl)ureido)benzoyl)-4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazine-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 1-(4-(3-(cyclopropylmethyl)ureido)benzoyl)-4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazine-2-carboxylate | HCID 59175829 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-(3-(Cyclopropylmethyl)ureido)benzoyl)-4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazine-2-carboxylic acid | HCID 59175886 | 83% |
Reaction Steps
Methyl 1-(4-(3-(cyclopropylmethyl)ureido)benzoyl)-4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazine-2-carboxylate (0.032 mmol, 0.02 g) and sodium hydroxide (0.032 mmol, 1.298 mg) were combined and heated to 80° C. in methanol (1 mL) for 6 hours in a reactivial. The reaction mixture was concentrated under reduced pressure. The resulting residue was passed down an SCX column to afford the title compound (16 mg). MS (ESI) m/z 603.2 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357679B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-6e9d1f73ae1a4916bbffd79fbbe3452f |
| Source note | uspto-grants-2013_01 |