Isopropylamine → 2-aminopyrido[2,3-d]pyrimidin-7(8H)-one 23

HRID 3185

反応式

HRID 3185 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:20](=[O:21])[N:19]([CH3:22])[C:12]2[N:13]=[C:14](SC)[N:15]=[CH:16][C:11]=2[CH:10]=1.[CH:23]([NH2:26])([CH3:25])[CH3:24]>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:20](=[O:21])[N:19]([CH3:22])[C:12]2[N:13]=[C:14]([NH:26][CH:23]([CH3:25])[CH3:24])[N:15]=[CH:16][C:11]=2[CH:10]=1

参加物

3

実験手順

This compound was prepared by a procedure similar to that described in Example 40 starting with 6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 37 and isopropylamine; mp 194°-196° C.

後処理

  1. customThis compound was prepared by a procedure similar to

出典と根拠

ORDレコード
ord-d04022b22bcd4100a137a9c7f735c157
出典データセット
uspto-grants-1998_03
特許番号
US05733914

関連ノート

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