Acetonitrile--water (1/1) → HCID 131719992, 화합물
반응식
[NH2:1][CH2:2][C@H:3]1[O:23][CH2:22][CH2:21][C@H:4]1[S:5][C:6]1[CH:12]([CH3:13])[CH:11]2[N:8]([C:9](=[O:17])[CH:10]2[CH:14]([OH:16])[CH3:15])[C:7]=1[C:18]([OH:20])=[O:19].P([O-])(O)(O)=O.[Na+].[C:30](#[N:32])[CH3:31].[OH2:33].[H][H]>O1CCOCC1.[Pd]>[NH2:32][CH:30]([CH:3]([CH3:2])[CH2:4][CH3:21])[C:31]([NH:1][CH2:2][C@H:3]1[O:23][CH2:22][CH2:21][C@H:4]1[S:5][C:6]1[CH:12]([CH3:13])[CH:11]2[N:8]([C:9](=[O:17])[CH:10]2[CH:14]([OH:16])[CH3:15])[C:7]=1[C:18]([OH:20])=[O:19])=[O:33]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
The title compound is prepared by the procedure of Example 257 using 0.342 g of product from Example 192 in 10 ml of pH 7 0.1M sodium dihydrogen phosphate buffer, 0.407 g of product from Example 299 in 7 ml of dioxane to give after chromatography (Reverse Phase plates: 25% acetonitrile/water) an oil. The oil is mixed with 0.10 g of 10% palladium on carbon, 10 ml of pH 7 0.1M sodium dihydrogen phosphate buffer and 5 ml of dioxane. The solution is reduced in a Parr apparatus at 47 psi of hydrogen for 3 hours, The reaction mixture is filtered, the filtrate is concentrated in vacuo to a small volume and purified by chromatography (Reverse phase plates: 25% acetonitrile/water) to give 0.090 g of the desired product.
후처리
- filtrationThe reaction mixture is filtered
- concentrationthe filtrate is concentrated in vacuo to a small volume
- custompurified by chromatography (Reverse phase plates: 25% acetonitrile/water)
출처 및 근거
- ORD 기록
- ord-121431a176514971af03680cb9a107b6
- 출처 데이터셋
- uspto-grants-1997_04
- 특허 번호
- US05623081
반응 노트
불러오는 중…