반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C@@H:8]([O:14]C(=O)N)[CH2:9][C:10]([N:12]=[O:13])=[O:11])[CH:5]=[CH:6][CH:7]=1.ClC1C=C([C@H](O)CO)C=CC=1>CO>[Cl:1][C:2]1[CH:3]=[C:4]([C@@H:8]([OH:14])[CH2:9][C:10]([N:12]=[O:13])=[O:11])[CH:5]=[CH:6][CH:7]=1참가 물질
4
실험 절차
(S)-(2-(3-Chlorophenyl)-2-carbamoyloxyethyl)oxocarboxamide (1.36 g, yield 25%, m.p. 117-119° C., [α]D =12.88 (c=2.30, MeOH) was prepared using the same synthetic method described in Example 20, except (S)-1-m-chlorophenyl-1,2-ethanediol was used instead of (DL)-1-m-chlorophenyl-1,2-ethanediol.
출처 및 근거
- ORD 기록
- ord-6cfca9cd125a4350a3f7dbb8723965ae
- 출처 데이터셋
- uspto-grants-2000_10
- 특허 번호
- US06127412
연결된 노트
불러오는 중…