Diisopropylethylamine → 4-Chloro-2-(cyclopropylmethyl-amino)-6-(2-hydroxy-ethylamino)-pyrimidine-5-carbonitrile
反応式
[Cl:1][C:2]1[C:7]([C:8]#[N:9])=[C:6]([NH:10][CH2:11][CH2:12][OH:13])[N:5]=[C:4](S(C)(=O)=O)[N:3]=1.N[C:19]1([CH3:22])C[CH2:20]1.[CH2:23]([N:25](C(C)C)C(C)C)C>O1CCOCC1>[Cl:1][C:2]1[C:7]([C:8]#[N:9])=[C:6]([NH:10][CH2:11][CH2:12][OH:13])[N:5]=[C:4]([NH:25][CH2:23][CH:22]2[CH2:19][CH2:20]2)[N:3]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
In analogy to the procedure described in example 47a, the crude 4-chloro-6-(2-hydroxy-ethylamino)-2-methanesulfonyl-pyrimidine-5-carbonitrile was treated with amino-methyl-cyclopropane in dioxane in the presence of N-ethyl-diisopropylamine at 40° C. to yield 4-chloro-2-(cyclopropylmethyl-amino)-6-(2-hydroxy-ethylamino)-pyrimidine-5-carbonitrile as an amorphous, white solid; MS: [M+H]+=268.
出典と根拠
- ORDレコード
- ord-b23fbded299947afbcc2a53865649dc8
- 出典データセット
- uspto-grants-2004_01
- 特許番号
- US06673795B2
反応ノート
読み込み中…