참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyrithione | HCID 1570 | — |
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 2,2'-Thiodipyridine | HCID 521114 | 72% |
반응 단계
360 mg (1 mmol) of peracetoquinic acid (32) are taken into solution with stirring in 5 ml of benzene with the addition of 1 ml of oxalyl chloride and 1 drop of DMF for 3 hours. After evaporation to dryness, the residue is taken up in 5 ml of benzene and added with stirring to a suspension of 180 mg (1.1 mmol) of the sodium salt of N-hydroxypyridine-2-thione and 12 mg (0.1 mmol) of DMAP. The reaction mixture is kept refluxing in 10 ml of toluuene under an atmosphere of nitrogen. After 2 hours of heating under reflux, the cooled reaction mixture is filtered on Celite and evaporated to dryness. By flash chromatography on silica (90% of CH2Cl2 ; 10% EtOAc), 306 mg of pyridyl sulfide of formula (34) are obtained in the form of a yellowish oil. Yield 72%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04668356 |
|---|
| 출처 데이터셋 | uspto-grants-1987_05 |
|---|
| ORD ID | ord-f97cda4dac004f19a4353661f6288300 |
|---|
| 출처 메모 | uspto-grants-1987_05 |
|---|