HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178481571, compound → HCID 178481569, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178481571 | HCID 178481571 | — |
| Reactant | HCID 178507567 | HCID 178507567 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178481569 | HCID 178481569 | — |
Reaction Steps
The title compound was prepared from Intermediate 3 and 3-[(tetrazol-5-yl)aminomethyl]aniline using a similar method to that described for Example 4, except that anhydrous acetonitrile was used instead of tetrahydrofuran; the crude product was purified by flash chromatography (silica gel, dichloromethane-methanol, 95:5 to 90:10) and recrystallized from a mixture of methanol and ethyl acetate; mp 175°-178° C.; [α]D24 +17.4° (c=0.50, dimethylformamide); the spectroscopic properties of this material (1 H-NMR and MS spectra) were identical to those described for its racemate (Example 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05681833 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-faad67cb2b5b4f99918d43941d43b365 |
| Source note | uspto-grants-1997_10 |