반응식
[NH:1]1[CH:5]=[C:4]([CH2:6][CH2:7]O)[CH:3]=[N:2]1.[NH2:9][C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:11]=1[SH:17].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CC(OC(/N=N/C(OC(C)(C)C)=O)=O)(C)C>C(Cl)Cl>[NH:1]1[CH:5]=[C:4]([CH2:6][CH2:7][S:17][C:11]2[CH:12]=[CH:13][C:14]([Cl:16])=[CH:15][C:10]=2[NH2:9])[CH:3]=[N:2]1참가 물질
6
실험 절차
Following the General Procedure J, the title intermediate was prepared from 2-(1H-pyrazol-4-yl) ethanol (472 mg, 4.218 mmol), 2-amino-4-chlorobenzenethiol (1.01 g, 6.327 mmol), PPh3 (2.21 g, 8.436 mmol) and di-tert-butylazodicarboxylate (1.9 g, 8.436 mmol) in CH2Cl2 (20 ml).
출처 및 근거
- ORD 기록
- ord-c8886a7c84de41818cd19b52db18dc58
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08822530B2
연결된 노트
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