N-(2-aminoethyl)acetamide → N-[2-(2-chloro-5-iodopyrimidine-4-ylamino)ethyl]acetamide

反応式

[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([I:9])=[CH:4][N:3]=1.[NH2:10][CH2:11][CH2:12][NH:13][C:14](=[O:16])[CH3:15]>>[Cl:1][C:2]1[N:7]=[C:6]([NH:10][CH2:11][CH2:12][NH:13][C:14](=[O:16])[CH3:15])[C:5]([I:9])=[CH:4][N:3]=1

参加物

反応物 2

HCID 66082N-(2-aminoethyl)acetamide

HCID 2634382,4-Dichloro-5-iodopyrimidine

生成物 1

HCID 59550867N-[2-(2-chloro-5-iodopyrimidine-4-ylamino)ethyl]acetamide収率 71%

実験手順

In analogy to GP 2 reaction of 2,4-dichloro-5-iodopyrimidine (1.0 g, 3.6 mmol) with N-(2-aminoethyl)acetamide (e.g. ABCR, Aldrich) (0.42 mL, 3.9 mmol) provided the desired product in 71% yield (878 mg) after trituration of the crystals obtained with diethyl ether.

出典と根拠

ORDレコード: ord-babe7f6101a14a28b4e9c3ffab25ca6a
出典データセット: uspto-grants-2013_09
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US08524724B2

反応ノート

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