반응식
[CH:1]1[C:13]2[CH:12]([CH2:14][O:15][C:16]([NH:18][C:19]3([C:25](O)=[O:26])[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]3)=[O:17])[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.C(C1NC=CN=1)(C1NC=CN=1)=O.Cl.Cl.[NH2:42][C:43]1[C:51]([NH2:52])=[CH:50][CH:49]=[CH:48][C:44]=1[C:45]([NH2:47])=[O:46].C(O)(C)C>N1C=CC=CC=1.CN(C=O)C>[CH:1]1[C:13]2[CH:12]([CH2:14][O:15][C:16](=[O:17])[NH:18][C:19]3([C:25](=[O:26])[NH:52][C:51]4[CH:50]=[CH:49][CH:48]=[C:44]([C:45](=[O:46])[NH2:47])[C:43]=4[NH2:42])[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]3)[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 40 °C
실험 절차
A solution of 1-(9H-fluoren-9-ylmethoxycarbonyl amino)-cyclohexanecarboxylic acid (0.326 g, 0.9 mmol) in pyridine (1 mL) and DMF (1 ml) was heated to 40° C. for 30 min. Carbonyl diimidazole (0.15 g, 0.9 mmol) was added and the mixture was stirred at 40° C. for 1 hour then treated with 2,3-diamino-benzamide dihydrochloride (prepared as described in WO0026192, 0.2 g, 0.9 mmol). After stirring for 1 hour at room temperature, isopropyl alcohol (3 ml) was added and the solution was cooled overnight at 0° C. The precipitated solid was filtered, dissolved in water (3 ml), treated with 50% aqueous NaOH (0.071 ml) then stirred for 3 hours at room temperature. The mixture was filtered and used immediately in Example 48B.
후처리
- stirringAfter stirring for 1 hour at room temperature
- temperaturethe solution was cooled overnight at 0° C
- filtrationThe precipitated solid was filtered
- dissolutiondissolved in water (3 ml)
- additiontreated with 50% aqueous NaOH (0.071 ml)
- stirringthen stirred for 3 hours at room temperature
- filtrationThe mixture was filtered
출처 및 근거
- ORD 기록
- ord-3c7f730b94f942349c7865919bff10b4
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07728026B2
연결된 노트
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