HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 88485782, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 14100520 | HCID 14100520 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 88485782 | HCID 88485782 | 104.7% |
Reaction Steps
A mixture of 2-(2-aminothiazol-4-yl)-2-(Z)-[diphenylmethyloxycarbonyl(3,4-dihydroxyphenyl)methyl]oxyiminoacetic acid (IIa) (779 mg, 1.5 mmol) [for the preparation of compound IIa see: Japan Kokai 88-99078 published 4/30/88], dicyclohexylcarbodiimide (DCC, 352 mg, 1.71 mmol), N-hydroxybenzotriazole (261 mg, 1.71 mmol) in tetrahydrofuran (THF) (6 ml) was stirred at room temperature for 1 hr and the resulting precipitate was filtered off. The filtrate was concentrated under reduced pressure to provide 1.00 gram (100%) of the activated ester IIIa.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05095012 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-ae4850675f1f44dc8dab18274660c476 |
| Source note | uspto-grants-1992_03 |