HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 131716295, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 14310112 | HCID 14310112 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 131716295 | HCID 131716295 | 39% |
Reaction Steps
A solution consisting of 100 mg (0.235 mmol) of 6-(N-carbobenzoxy-L-phenylalanylamino)quinoline (Brynes, et al., 1981), 204 1 of allyl bromide, and 0.5 ml of dimethylformamide was allowed to react at room temperature for 48 h and at 50° C. for 12 h. Crude product was isolated by precipitation with ether followed by two ether washes. The compound was purified by dissolving the solid in water at 50° C., filtering the undissolved material and lyophilizing to obtain pure XVI. Recrystallization from ethanol/ethyl acetate yielded 50 mg (39% yield): mp 160° C. decomposes, 219° C. melts;Rf(E)=0.08. Fast atom bombardment mass spectrum of XVI: calculated for MW (466)+Br-. Found 466 (M=).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04897444 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-a311db44c77f4574bdb302a7a918f745 |
| Source note | uspto-grants-1990_01 |