Cyclohexylamine → 4-Fluoro-piperidine-4-carboxylic acid cyclohexylamide
반응식
C(OC([N:8]1[CH2:13][CH2:12][C:11]([F:17])([C:14]([OH:16])=O)[CH2:10][CH2:9]1)=O)(C)(C)C.[CH:18]1([NH2:24])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1.C(OC(N1CCC(C(=O)NC2CCCCC2)CC1)=O)(C)(C)C>>[CH:18]1([NH:24][C:14]([C:11]2([F:17])[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]2)=[O:16])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1참가 물질
4
실험 절차
The title compound is prepared according to the reaction sequence 3.01a-2.01b described above using 1-(tert-butoxycarbonyl)-4-fluoropiperidine-4-carboxylic acid instead of 1-(tert-butoxycarbonyl)-piperidine-4-carboxylic acid and cyclohexylamine as in 3.01a: LC-MS A: tR=0.49 min; [M+H]+=229.25.
출처 및 근거
- ORD 기록
- ord-a602ce92eed647648d6b9531ff0a0e0a
- 출처 데이터셋
- uspto-grants-2016_08
- 특허 번호
- US09428456B2
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