3-(Phenylmethoxy)benzenemethanol → 2-{[3-(Benzyloxy)Benzyl]Oxy}-6-Chloropyrazine
반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH2:12][OH:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:17][C:18]1[CH:23]=[N:22][CH:21]=[C:20](Cl)[N:19]=1>>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH2:12][O:13][C:20]1[CH:21]=[N:22][CH:23]=[C:18]([Cl:17])[N:19]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
3
실험 절차
The title compound was prepared according to the procedure of example 50, step 1, starting from 3-benzyloxybenzyl alcohol (3.46 g, 16.2 mmol), K-t-BuO (1.69 g, 15.1 mmol) and 2,6-dichloropyrazine (1.97 g, 13.2 mmol). The yield of the title compound was 2.64 g (61%) and was obtained as a semisolid. Anal. (C18H15ClN2O2) C, H, N.
후처리
- customThe title compound was prepared
- customwas obtained as a semisolid
출처 및 근거
- ORD 기록
- ord-f657dee9892e4e62ae6b81ae45bc7bac
- 출처 데이터셋
- uspto-grants-2003_07
- 특허 번호
- US06593330B2
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