반응식
[ClH:1].[CH:2]1[C:15]2[CH:14]=[C:13]([CH2:16][NH:17][C@@:18]([CH3:24])([C@@H:21]([OH:23])C)[CH2:19][OH:20])[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[C:6]=2[CH:5]=[CH:4][CH:3]=1.C1C2C=[C:36]([CH:39]=[O:40])C3C(=CC=CC=3)C=2C=CC=1.Cl.NC(COCC)(CO)CO>>[ClH:1].[CH2:39]([O:40][CH2:24][C:18]([NH:17][CH2:16][C:13]1[C:12]2[C:7]([C:6]3[CH:5]=[CH:4][CH:3]=[CH:2][C:15]=3[CH:14]=1)=[CH:8][CH:9]=[CH:10][CH:11]=2)([CH2:21][OH:23])[CH2:19][OH:20])[CH3:36]참가 물질
4
반응물 3
생성물 1
실험 절차
Using the reductive amination procedure outlined for 7G, phenanthrene-9-carbaldehyde (Aldrich) and 2-amino-2-ethoxymethyl-1,3-propanediol hydrochloride.1/4H2O (8B) gave 2-ethoxymethyl-2-(((9-phenanthrenyl)methyl)amino)-1,3-propanediol hydrochloride mp 173°-175°, (EtOH/Et2O), (C, H, Cl, N).
출처 및 근거
- ORD 기록
- ord-2d3f18eec6094fc68773a16b800e3f2b
- 출처 데이터셋
- uspto-grants-1989_02
- 특허 번호
- US04808625
연결된 노트
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