HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 178431927, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 2-(2-[2-Aminoethoxy]phenyl)acetic acid | HCID 13998438 | — |
| Reactant | HCID 178431949 | HCID 178431949 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178431927 | HCID 178431927 | 64% |
Reaction Steps
The title compound is prepared in 64% yield from 2-(2-[2-aminoethoxy]phenyl)acetic acid (U.S. Pat. No. 3,759,905) and 6-amino-2,2-dimethyl-3-(5-tetrazolyl)penam, by a procedure analogous to that of Example LXXXV. IR (KBr disc): 1780 cm-1 (β-lactam) and 1667 cm-1 (amide I). NMR (in D2O): 7.1 ppm (m, 4H), 5.7 ppm (d, 1H), 5.5 ppm (d, 1H), 5.2 ppm (s, 1H), 3.7-3.3 ppm (m, 4H), 3.1 ppm (q, 12H), 1.6 ppm (s, 3H), 1.2 ppm (t, 18H), 1.0 ppm (s, 3H). The product is a 1:2 complex of the title compound and triethylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04143039 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-87bfe01513084929b26040142f0cf4a8 |
| Source note | uspto-grants-1979_03 |