Piperazine → 6'-(6-Fluoro-pyridin-2-ylmethoxy)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl

HRID 2182139ノート

反応式

HRID 2182139 の反応式
Cl[C:2]1[CH:7]=[N:6][CH:5]=[C:4]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[N:11]=2)[N:3]=1.[NH:17]1[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1>>[F:16][C:12]1[N:11]=[C:10]([CH2:9][O:8][C:4]2[N:3]=[C:2]([N:17]3[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]3)[CH:7]=[N:6][CH:5]=2)[CH:15]=[CH:14][CH:13]=1

参加物

3

実験手順

Following the general procedure for the preparation of I-3b above, 2-chloro-6-(6-fluoro-pyridin-2-ylmethoxy)-pyrazine (100 mg, 0.42 mmol) and piperazine (360 mg, 4.17 mmol) were reacted to give the title compound (3-B). The crude material was purified by preparative TLC using 5% methanol/methylene chloride with 1% NH4OH as the eluant to yield 23 mg of the title product (3-B).

後処理

  1. customwere reacted

出典と根拠

ORDレコード
ord-85d3a5265f5345b6a81cf4b21783202a
出典データセット
uspto-grants-2005_05
特許番号
US06894050B2

反応ノート

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