7,8,9,10-Tetrahydro-8-methyl-2,3-bis(phenylmethoxy)-pyrido[4,3-f]quinoxalin-6-yl phosphonic acid diethyl ester → 1,2,3,4,7,8,9,10-Octahydro-8-methyl-2,3-dioxopyrido[4,3-f]quinoxalin-6-yl phoshonic acid diethyl ester
반응식
[CH2:1]([O:3][P:4]([C:9]1[C:10]2[CH2:38][N:37]([CH3:39])[CH2:36][CH2:35][C:11]=2[C:12]2[N:13]=[C:14]([O:27]CC3C=CC=CC=3)[C:15]([O:19]CC3C=CC=CC=3)=[N:16][C:17]=2[CH:18]=1)(=[O:8])[O:5][CH2:6][CH3:7])[CH3:2]>C(O)(=O)C.[Pd]>[CH2:6]([O:5][P:4]([C:9]1[C:10]2[CH2:38][N:37]([CH3:39])[CH2:36][CH2:35][C:11]=2[C:12]2[NH:13][C:14](=[O:27])[C:15](=[O:19])[NH:16][C:17]=2[CH:18]=1)(=[O:8])[O:3][CH2:1][CH3:2])[CH3:7]참가 물질
4
반응물 1
생성물 1
시약·촉매·용매 2
실험 절차
A solution of the compound from Example 105 (0.34 g, 0.65 mmol) was dissolved in 60 mL of acetic acid and hydrogenated at 52 psi over 20% Pd/C. The reaction mixture was filtered and concentrated. The residue was dissolved in EtOH (3 mL) and concentrated. This procedure was repeated several times. The residue was then dissolved in EtOH and triturated with ethyl acetate. The solid which formed was collected by suction filtration and dried under vacuum to give the title compound as a yellow solid (0.20 g, 83% yield) mp 310-330° C. (dec).
후처리
- filtrationThe reaction mixture was filtered
- concentrationconcentrated
- dissolutionThe residue was dissolved in EtOH (3 mL)
- concentrationconcentrated
- dissolutionThe residue was then dissolved in EtOH
- customtriturated with ethyl acetate
- customThe solid which formed
- filtrationwas collected by suction filtration
- customdried under vacuum
출처 및 근거
- ORD 기록
- ord-9322d0d46fa741b8997da5a7a5c5355d
- 출처 데이터셋
- uspto-grants-2004_03
- 특허 번호
- US06703391B2
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