Sodium borohydride → HCID 13911618, 화합물
반응식
[S:1]1[C:5]2[S:6](=[O:11])(=[O:10])[CH2:7][CH:8]=[CH:9][C:4]=2[CH:3]=[C:2]1[S:12]([NH2:15])(=[O:14])=[O:13].[OH2:16].Cl([O-])(=O)=[O:18].[Ba+2].Cl([O-])(=O)=O.[BH4-].[Na+]>O1CCCC1.O.[Os](=O)(=O)(=O)=O>[OH:16][CH:9]1[CH:8]([OH:18])[CH2:7][S:6](=[O:10])(=[O:11])[C:5]2[S:1][C:2]([S:12]([NH2:15])(=[O:13])=[O:14])=[CH:3][C:4]1=2참가 물질
반응 조건
- 온도
- 45 °C
실험 절차
A solution of 6H-thieno[2,3-b]thiopyran-2-sulfonamide-7,7-dioxide (1.15 g, 0.0043 m) in tetrahydrofuran (20 ml) was added to a stirred solution of barium chlorate monohydrate (2.23 g, 0.0069 m) in water (20 ml) under a nitrogen atmosphere. Osmium tetroxide (0.66 g, 0.0026 m) was added and the mixture was stirred at 45° C. for 22 hours. Sodium borohydride (0.16 g, 0.0043 m) was added portionwise and the mixture was stirred at ambient temperature for one hour. After filtering through "Super-Cel", the filtrate was concentrated under reduced pressure at 30° C. to remove tetrahydrofuran, the aqueous suspension was acidified with 6N hydrochloric acid (1.0 ml) and extracted with ethyl acetate (3×75 ml). The combined extracts were washed twice with water, dried over sodium sulfate and concentrated in vacuo to yield 0.81 g (63% yield) of crude product which was purified by chromatography on silica gel, eluting with 15% methanol-chloroform. Recrystallization from nitromethane afforded an analytical sample melting at 182.5°-185° C.
후처리
- stirringthe mixture was stirred at ambient temperature for one hour
- filtrationAfter filtering through "Super-Cel"
- concentrationthe filtrate was concentrated under reduced pressure at 30° C.
- customto remove tetrahydrofuran
- extractionextracted with ethyl acetate (3×75 ml)
- washThe combined extracts were washed twice with water
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-419cdc8b03434c2d9b307bca9086a8ac
- 출처 데이터셋
- uspto-grants-1987_06
- 특허 번호
- US04677115
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