반응식
ClC1N=C(C2C=CC=CC=2)N=C(OCCC(C)C)C=1.ClC1C=C(Cl)N=C(C2C=CC=CC=2)N=1.Cl[C:35]1[CH:40]=[C:39]([Cl:41])[N:38]=[C:37]([CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH3:51])[N:36]=1.[CH2:52]([CH:54]([CH2:57][CH2:58][CH2:59][CH3:60])[CH2:55][OH:56])[CH3:53]>CC(C)CCO>[Cl:41][C:39]1[N:38]=[C:37]([CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH3:51])[N:36]=[C:35]([O:56][CH2:55][CH:54]([CH2:52][CH3:53])[CH2:57][CH2:58][CH2:59][CH3:60])[CH:40]=1참가 물질
6
실험 절차
The compound of Example 25 is prepared analogously to the compound of Example 3, with 4,6-dichloro-2-phenylpyrimidine being replaced by 4,6-dichloro-2-decylpyrimidine and 3-methylbutanol by 2-ethylhexanol.
출처 및 근거
- ORD 기록
- ord-8f2f6752d00a4b1cbfe845f6a045f01c
- 출처 데이터셋
- uspto-grants-1994_08
- 특허 번호
- US05340701
연결된 노트
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