HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (4-Hydroxymethyl-5-fluoro-thiazol-2-yl)-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thiazole-4-carboxaldehyde | HCID 2763214 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | 2-(tert-butoxycarbonylamino)-4-(N-methoxy-N-methyl-aminomethyl)-5-fluorothiazole | HCID 58055049 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Hydroxymethyl-5-fluoro-thiazol-2-yl)-carbamic acid tert-butyl ester | HCID 86647350 | 45% |
Reaction Steps
A solution of Intermediate 104: {5-Fluoro-4-[(methoxy-methyl-amino)-methyl]-thiazol-2-yl}-carbamic acid tert-butyl ester (7.5 g, 25.7 mmol) in THF (45 mL) and water (4.5 mL) was rapidly stirred and treated slowly dropwise with 6.15% sodium hypochlorite solution in water (Clorox™, 67 mL, 55 mmol). The resulting thiazole-4-carboxaldehyde was reduced in situ with sodium borohydride (0.5 g). The reaction was acidified with 2 N HCl (10 mL) and extracted with diethyl ether (2×50 mL). The extracts were dried with sodium sulfate and evaporated to leave an orange resin which purified by silica gel chromatography (80% EtOAc/hexane) to afford (4-hydroxymethyl-5-fluoro-thiazol-2-yl)-carbamic acid tert-butyl ester as a yellow foam (2.9 g, 45% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08293919B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-56ce5b0f06204018890156781e93cacd |
| Source note | uspto-grants-2012_10 |