2,4-Dichloro-5-fluoropyrimidine → 2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamine

HRID 226593

反応式

HRID 226593 の反応式
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([F:9])=[CH:4][N:3]=1.[NH2:10][C:11]1[CH:20]=[C:19]2[C:14]([CH2:15][CH2:16][CH2:17][C:18]2=[O:21])=[CH:13][CH:12]=1>>[Cl:1][C:2]1[N:7]=[C:6]([NH:10][C:11]2[CH:20]=[C:19]3[C:14]([CH2:15][CH2:16][CH2:17][C:18]3=[O:21])=[CH:13][CH:12]=2)[C:5]([F:9])=[CH:4][N:3]=1

参加物

3

反応物 2

HCID 2507052,4-Dichloro-5-fluoropyrimidineHCID 3271777-Amino-1,2,3,4-tetrahydronaphthalen-1-one

生成物 1

HCID 220607872-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamine

実験手順

In a like manner to the preparation of 2-chloro-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-4-pyrimidineamine, 2,4-dichloro-5-fluoropyrimidine and 7-amino-1-tetralone were reacted to provide 2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamine. 1H NMR (DMSO-d6): δ 10.08 (s, 1H), 8.31 (d, 1H, J=3.3 Hz), 8.15 (d, 1H, J=2.4 Hz), 7.82 (dd, 1H, J=2.4 and 8.1 Hz), 7.36 (d, 1H, J=8.1 Hz), 2.91 (t, 2H, J=6.0 Hz), 2.59 (t, 2H, J=6.0 Hz), 2.07–1.98 (m, 2H); LCMS: purity: 93%; MS (m/e): 294(MH+).

後処理

  1. customwere reacted

出典と根拠

ORDレコード
ord-2bca8b203b714fc09596e341940ea847
出典データセット
uspto-grants-2009_07
特許番号
US07557210B2

関連ノート

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