Diisopropylethylamine → HCID 58098673、化合物

HRID 533481

反応式

HRID 533481 の反応式
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:4][N:3]=1.[CH3:14][N:15]1[CH:19]=[C:18]([CH2:20][NH2:21])[CH:17]=[N:16]1.CCN(C(C)C)C(C)C>CC#N>[Cl:1][C:2]1[N:7]=[C:6]([NH:21][CH2:20][C:18]2[CH:17]=[N:16][N:15]([CH3:14])[CH:19]=2)[C:5]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:4][N:3]=1

参加物

5

反応物 3

HCID 81531DiisopropylethylamineHCID 104020Ethyl 2,4-dichloropyrimidine-5-carboxylateHCID 671225(1-methyl-1H-pyrazol-4-yl)methanamine

生成物 1

HCID 58098673HCID 58098673、化合物

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a solution of ethyl 2,4-dichloropyrimidine-5-carboxylate (896 mg, 4 mmol) and (1-methyl-1H-pyrazol-4-yl)methanamine (445 mg, 4 mmol) in CH3CN (6 mL) at room temperature, DIEA (0.783 mL, 4.4 mmol) was added. The mixture was stirred at room temperature for 24 h, and was concentrated to give ethyl 2-chloro-4-((1-methyl-1H-pyrazol-4-yl)methylamino)pyrimidine-5-carboxylate as crude oil.

後処理

  1. concentrationwas concentrated

出典と根拠

ORDレコード
ord-49d059b67d2d4e329eaa578509d7ca48
出典データセット
uspto-grants-2014_10
特許番号
US08853230B2

関連ノート

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