반응식
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][NH2:8])=[CH:3][CH:2]=1.[Cl:9][CH2:10][CH2:11][O:12][CH2:13][CH2:14][C:15](Cl)=[O:16]>>[Cl:9][CH2:10][CH2:11][O:12][CH2:13][CH2:14][C:15]([NH:8][CH2:7][C:4]1[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=1)=[O:16]참가 물질
3
실험 절차
Title compound was prepared starting from (4-pyridyl)methanamine and 3-(2-chloroethoxy)propanoyl chloride following the procedure outlined for Example 27A. 1H NMR (CDCl3): δ 2.38-2.41 (m, 2H), 2.60-2.63 (m, 2H), 3.54-3.60 (m, 2H), 3.66-3.69 (m, 2H), 4.45 (d, 2H, J=6.1 Hz), 6.12 (br t, 1H, D2O exchanged), 7.09-7.11 (m, 2H), 8.40-8.42 (m, 2H).
출처 및 근거
- ORD 기록
- ord-41ba896a75c548f680f4658c146109c1
- 출처 데이터셋
- uspto-grants-2016_02
- 특허 번호
- US09260400B2
연결된 노트
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