3-Iodopicolinic acid → (3-Iodopyridin-2-yl)methanol
반응식
[I:1][C:2]1[C:3]([C:8](O)=[O:9])=[N:4][CH:5]=[CH:6][CH:7]=1.ClC1C(CO)=CC(F)=C(Cl)N=1>>[I:1][C:2]1[C:3]([CH2:8][OH:9])=[N:4][CH:5]=[CH:6][CH:7]=1참가 물질
3
실험 절차
Compound 51A (10 mg, 10%) was prepared from 3-iodo-pyridine-2-carboxylic acid (100 mg, 0.4 mmol) ) using a procedure similar to the synthesis of 1A. HPLC Rt=0.3 min
출처 및 근거
- ORD 기록
- ord-d37374855e164e74b6f18014674ccef6
- 출처 데이터셋
- uspto-grants-2008_05
- 특허 번호
- US07378426B2
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