HCID 14208511, 화합물 → HCID 57112142, 화합물
반응식
[CH2:1]([O:8][C:9]1[C:16]([O:17][CH2:18]C)=[CH:15][CH:14]=[C:13]([N+]([O-])=O)[C:10]=1[CH:11]=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC1C(OC)=CC=[C:35]([N+:41]([O-:43])=[O:42])[C:32]=1C=O)C1C=CC=CC=1>>[CH2:1]([O:8][C:9]1[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[C:13]([CH2:35][N+:41]([O-:43])=[O:42])[C:10]=1[CH:11]=[CH:32][CH2:35][N+:41]([O-:43])=[O:42])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
3
실험 절차
This compound is obtained according to the operating method described in Example 2a, in which the 2-benzyloxy-3-ethoxy-6-nitrobenzaldehyde is replaced with 2-benzyloxy-3-methoxy-6-nitrobenzaldehyde. A light yellow powder (yield=53%, m.p.=149°-150° C.) is obtained.
후처리
- customThis compound is obtained
출처 및 근거
- ORD 기록
- ord-6ed4976ddcbb4fad875e04d5a7998cbe
- 출처 데이터셋
- uspto-grants-1992_07