HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 54272787, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(4-Tert-butoxycarbonylamino-phenyl)-3-[(5-methyl-isoxazole-3-carbonyl)-amino]-propionic acid tert-butyl ester | HCID 53886303 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54272787 | HCID 54272787 | 64.5% |
Reaction Steps
A solution of (R) 3-(4-tert-butoxycarbonylamino-phenyl)-3-[(5-methyl-isoxazole-3-carbonyl)-amino]-propionic acid tert-butyl ester (2 g, Reference Example 11) in dichloromethane (50 mL) was treated with trifluoroacetic acid (5 mL). After four hours [the reaction was monitored by TLC: no more starting material was visible after about 4 hours] at room temperature the reaction mixture was poured carefully onto a mixture of sodium hydrogen carbonate solution (100 mL, 5% w/v) and dichloromethane (50 mL). The organic layer was separated then dried and then evaporated to give the title compound (1.0 g) as a yellow oil which slowly crystallised on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562851B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-2847da8ee73547e7bb470155cde7cae1 |
| Source note | uspto-grants-2003_05 |