Lithium hexamethyldisilazane → 7-(7-Hydroxy-6-oxo-2,3-dip-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoic acid

온도

-10 °C

To a solution of 7-(6-oxo-2,3-dip-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoic acid (Ex. 12.1) (100 mg, 0.219 mmol) in THF (2 ml), under a nitrogen atmosphere at −78° C., was treated dropwise with 1M lithium bis trimethylsilylamide in THF (0.5 ml, 0.500 mmol). Once the addition was complete, the mixture was stirred at −78° C. for 1 hour before a solution of (+)-(8,8-dichlorocamphorylsulfonyl)oxaziridine (78 mg, 0.262 mmol) in THF (2 ml) was added. The resultant solution was stirred at −78° C. for 60 minutes. The cooling was removed and the mixture allowed to warm to around −10° C. The mixture was allowed to slowly warm to room temperature overnight. The mixture was cooled to −78° C., quenched with sat. NH4Cl (3 ml) and allowed to slowly warm to room temperature. The yellow solution was diluted with water and extracted with EtOAc (×2). The aqueous layer (pH-9) was acidified to pH ˜2 with 1M HCl and extracted with DCM (×2). The combined organic extracts were dried (MgSO4) and evaporated under vacuum to give a yellow gum. The residue was purified by chromatography on silica eluting with 1% MeOH/DCM followed by 10% MeOH/DCM to afford the title compound;

1. additionOnce the addition
2. additionwas added
3. customThe cooling was removed
4. temperatureto slowly warm to room temperature overnight
5. temperatureThe mixture was cooled to −78° C.
6. customquenched with sat. NH4Cl (3 ml)
7. temperatureto slowly warm to room temperature
8. additionThe yellow solution was diluted with water
9. extractionextracted with EtOAc (×2)
10. extractionextracted with DCM (×2)
11. dry with materialThe combined organic extracts were dried (MgSO4)
12. customevaporated under vacuum
13. customto give a yellow gum
14. customThe residue was purified by chromatography on silica eluting with 1% MeOH/DCM

ORD 기록

ord-97a7a96848dc402199fd43812bb45c25

출처 데이터셋

uspto-grants-2015_09

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US09132127B2