N-(1-Methylethyl)-1-decanamine → HCID 57094078、化合物
反応式
C(N(CCCCCCCCC)[C:7](=[O:16])[NH:8][C@H:9]1[CH2:14][CH2:13][CH2:12][CH2:11][C@@H:10]1[OH:15])C(C)(C)C.C(NCCCCCCCCC)C(C)(C)C.[CH2:41]([NH:51][CH:52]([CH3:54])[CH3:53])[CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH3:50]>>[CH2:41]([N:51]([CH:52]([CH3:53])[CH3:54])[C:7](=[O:16])[NH:8][C@H:9]1[CH2:14][CH2:13][CH2:12][CH2:11][C@@H:10]1[OH:15])[CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH3:50]参加物
4
実験手順
The same procedure for preparing (1S,2S)-2-(3-neopentyl-3-nonylureido)cyclohexanol as in Example 3 was repeated except that the neopentylnonylamine employed in Example 3 was replaced by decylisopropylamine, whereby (1S,2S)-2-(3-decyl-3-isopropylureido)cyclohexanol was obtained in a yield of 88%.
出典と根拠
- ORDレコード
- ord-25fe3a4c1269444d8848add9b0b54682
- 出典データセット