HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 13473425, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 3-{N-[beta-(3,4-Dipivalyloxyphenyl)ethyl]}carbamoylpyridine | HCID 13473420 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13473425 | HCID 13473425 | — |
Reaction Steps
To a solution of 5.0 g (11.7 mmol) of compound 8c in 20 ml of acetone, 3.3 g (23.4 mmol) of methyl iodide were added and the mixture was refluxed under stirring for 6 hrs, then cooled. The orange crystalline solid which separated was filtered, washed with ether and crystallized for acetone/ether. Yield, 5.6 g (85%), m.p. 163°-165° C. U.V. (buffer pH 7.4) 270, 215 nm. NMR (DMSO-d6) δ7.68-7.06 (ms, 7H, ##STR1468## +C6H3 +NH), 4.56 3.42 (q, 2H, J=7 Hz, --N--CH2), 3.19 (t, 2H, J=7 Hz, CH2), 1.32 (s, 18H, `--C(CH3)3). Anal. Calcd for C25H33IN2O5 : C, 52.82; H, 5.85; N, 4.92. found: C, 52.76; H, 5.87; N, 4.90.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05008257 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-8a22b3e399894900b44be5d82dd68d21 |
| Source note | uspto-grants-1991_04 |