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Diethyl Ether → Diethyl (4-{[4-chloro-5-(trifluoromethyl)pyrimidin-2-yl]amino}-3-fluorobenzyl)phosphonate

HRID 2279767
ノート
印刷プレビュー

反応式

HRID 2279767 の反応式
Cl[C:2]1[N:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[C:4]([Cl:12])[N:3]=1.CCOCC.[CH2:18]([O:20][P:21]([CH2:26][C:27]1[CH:32]=[CH:31][C:30]([NH2:33])=[C:29]([F:34])[CH:28]=1)(=[O:25])[O:22][CH2:23][CH3:24])[CH3:19].C(N(C(C)C)CC)(C)C>ClC(Cl)C.C(O)(C)(C)C.[Cl-].[Zn+2].[Cl-]>[Cl:12][C:4]1[C:5]([C:8]([F:11])([F:10])[F:9])=[CH:6][N:7]=[C:2]([NH:33][C:30]2[CH:31]=[CH:32][C:27]([CH2:26][P:21](=[O:25])([O:20][CH2:18][CH3:19])[O:22][CH2:23][CH3:24])=[CH:28][C:29]=2[F:34])[N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 3283Diethyl EtherHCID 81531DiisopropylethylamineHCID 27827742,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 86697720(4-Amino-3-fluorobenzyl)phosphonic acid diethyl ester2 回

生成物 1

HCID 86697719Diethyl (4-{[4-chloro-5-(trifluoromethyl)pyrimidin-2-yl]amino}-3-fluorobenzyl)phosphonate収率 111.2%

試薬・触媒・溶媒 3

HCID 3007855Zincchloride触媒HCID 63651,1-Dichloroethane溶媒2 回HCID 6386tert-Butanol溶媒2 回

実験手順

A solution of 2,6-Dichloro-5-trifluoromethylpyrimidine (4.76 gm, 22 mmol) in 20 mL of dichloroethane and t-butanol (1:1) was treated with a 1M solution of zinc chloride in ether (22 mL, 22 mmol) and allowed to stir at RT for 30 minutes. The mixture was subsequently cooled to 0° C. and treated with a solution of (4-amino-3-fluorobenzyl)phosphonic acid diethyl ester (Compound 22D, 3.3 g, 7.94 mmol) in dichloroethane and t-butanol (10 mL, 1:1) over 10 min through an addition funnel. After 1 hr, diisopropylethylamine (2.2 mL, 12.6 mmol) was added and the mixture was allowed to stir for 24 hours at RT. The solvents were evaporated and the residue was purified using flash column chromatography (9:1 DCM:EtOAc) to afford 3.9 g of the title compound (71%). 1H NMR (600 MHz, CDCl3): δ=1.23-1.28 (m, 6H), 3.1 (d, J=22 Hz, 2H), 4.02-4.09 (m, 4H), 7.09-7.25 (m, 2H), 7.63 (s, 1H), 8.24-8.27 (m, 1H), 8.58 (s, 1H).

後処理

  1. temperatureThe mixture was subsequently cooled to 0° C.
  2. waitAfter 1 hr
  3. stirringto stir for 24 hours at RT
  4. customThe solvents were evaporated
  5. customthe residue was purified

出典と根拠

ORDレコード
ord-8a08f26cd1b34620a04bb5cedf8305e7
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09133224B2

反応ノート

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