반응식
[C:1]([N:20]1[CH:24]=[C:23]([CH2:25][OH:26])[CH:22]=[N:21]1)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].I[CH3:30]>O1CCCC1>[C:1]([N:20]1[CH:24]=[C:23]([CH2:25][O:26][CH3:30])[CH:22]=[N:21]1)([C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1참가 물질
5
실험 절차
This compound is obtained by reacting 1-trityl-4-hydroxymethylpyrazole (555 mg; 1.63 mmol) in dry tetrahydrofuran with sodium hydride (98 mg; 2.44 mmol) and iodomethane (0.5 mL; 8.15 mmol). Yield: 93° A) (536 mg, 1.51 mmol).
후처리
- customThis compound is obtained
출처 및 근거
- ORD 기록
- ord-1e7f6f99d4d941298199338d23075d71
- 출처 데이터셋
- uspto-grants-2013_02
- 특허 번호
- US08372379B2
연결된 노트
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