HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Tert-butoxycarbonylamino-5-[(3-carboxyphenyl)thio]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Tert-butoxycarbonylamino-5-[(3-carbomethoxyphenyl)thio]thiazole | HCID 22170410 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 2-Tert-butoxycarbonylamino-5-[(3-carboxyphenyl)thio]thiazole | HCID 22170420 | — |
Reaction Steps
A 1 N aqueous sodium hydroxide solution (50 mL, 50 mmol) was added dropwise to a stirred solution of 2-tert-butoxycarbonylamino-5-[(3-carbomethoxyphenyl)thio]thiazole (1.8 g, (contaminated with bis(tert-butoxycarbonyl)amino adduct)) in a methanol-THF mixture (160 mL, 3:1). The solution was stirred at rt. for 24 h and concentrated. The residue was acidified with 2 N aqueous HCl (30 mL) and the suspension was extracted with dichloromethane-methanol mixture (120 mL, 3:1, 2×). The combined organic extract was dried (MgSO4), filtered and concentrated in vacuo to obtain the titled compound (1.32 g, 75% overall yield from Example 1, part A) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706717B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-dcaf7ef49c6e461b954ec64cb251cdb9 |
| Source note | uspto-grants-2004_03 |