HCID 58289789、化合物 → HCID 58290015、化合物

HRID 2088755

反応式

HRID 2088755 の反応式
[CH3:1][C:2]1([CH3:13])[C:11]2[C:6](=[CH:7][C:8]([NH2:12])=[CH:9][CH:10]=2)[CH2:5][NH:4][CH2:3]1.Cl[C:15]1[N:20]=[C:19]2[N:21]([CH3:35])[C:22](=[O:34])[N:23]([C:26]3[C:31]([Cl:32])=[CH:30][CH:29]=[CH:28][C:27]=3[Cl:33])[C:24](=[NH:25])[C:18]2=[CH:17][N:16]=1.ClC1N=C2NC(=O)N(C3C(Cl)=CC=CC=3Cl)C(=N)C2=CN=1>>[Cl:32][C:31]1[CH:30]=[CH:29][CH:28]=[C:27]([Cl:33])[C:26]=1[N:23]1[C:24](=[NH:25])[C:18]2[C:19](=[N:20][C:15]([NH:12][C:8]3[CH:7]=[C:6]4[C:11]([C:2]([CH3:13])([CH3:1])[CH2:3][NH:4][CH2:5]4)=[CH:10][CH:9]=3)=[N:16][CH:17]=2)[N:21]([CH3:35])[C:22]1=[O:34]

参加物

4

実験手順

160 mg of the entitled compound was obtained as a white solid according to the same method as in Example 2, for which, however, 4,4-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-amine was used in place of 2,4,4-trimethyl-1,2,3,4-tetrahydroisoquinolin-7-amine in Example 2, and 7-chloro-3-(2,6-dichlorophenyl)-4-imino-1-methyl-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one obtained in Production Example 7 was used in place of 7-chloro-3-(2,6-dichlorophenyl)-4-imino-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one.

後処理

  1. customobtained in Production Example 7

出典と根拠

ORDレコード
ord-83dd1bb58d8446878e24d4dbc2628533
出典データセット
uspto-grants-2013_05
特許番号
US08436004B2

関連ノート

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