Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86637987 | HCID 86637987 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44548736 | HCID 44548736 | 54.4% |
Reaction Steps
To a stirred solution of N-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-methyl-1H-indol-3-yl]methyl}-D-alaninate (D80) (110 mg) in THF (2 mL) was added aqueous NaOH (2 M, 2 mL). The reaction was stirred at room temperature overnight. The reaction mixture was acidified with HCl (2 M) to pH 6-7. The resulting solid was separated and suspended in methanol (2 mL) with stirring, HCl (2M) was added until the solid dissolved completely. The solution was freeze dried to afford N-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-methyl-1H-indol-3-yl]methyl}-D-alanine (E59) (60 mg, HCl salt). δH (DMSO-d6, 400 MHz): 1.35 (6H, d), 1.48 (3H, d), 3.71 (3H, s), 3.86 (1H, q), 4.35 (2H, s), 4.89 (1H, m), 7.28 (1H, t), 7.45 (1H, d), 7.51 (1H, d), 7.60 (1H, s), 8.03 (1H, d), 8.13 (1H, d), 8.20 (1H, s). MS (ES): C24H26ClN4O4 requires 468; found 380.1 (M—C3H6NO2+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08217028B2 |
|---|
| Source dataset | uspto-grants-2012_07 |
|---|
| ORD ID | ord-c54a7016cd644b0d99dce93dd4e3154c |
|---|
| Source note | uspto-grants-2012_07 |
|---|