2,4-Difluoroaniline → 2-Chloro-N-(2,4-difluorophenyl)-4-iodonicotinamide

HRID 1986088ノート

反応式

HRID 1986088 の反応式
[Cl:1][C:2]1[N:10]=[CH:9][CH:8]=[C:7]([I:11])[C:3]=1[C:4]([OH:6])=O.[F:12][C:13]1[CH:19]=[C:18]([F:20])[CH:17]=[CH:16][C:14]=1[NH2:15].C1CN([P+](Br)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CN(C=O)C>[Cl:1][C:2]1[N:10]=[CH:9][CH:8]=[C:7]([I:11])[C:3]=1[C:4]([NH:15][C:14]1[CH:16]=[CH:17][C:18]([F:20])=[CH:19][C:13]=1[F:12])=[O:6]

参加物

6

反応物 4

HCID 97092,4-DifluoroanilineHCID 81531DiisopropylethylamineHCID 2733179PyBroPHCID 177501742-Chloro-4-iodonicotinic acid

生成物 1

HCID 577213332-Chloro-N-(2,4-difluorophenyl)-4-iodonicotinamide収率 54.5%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a homogeneous mixture of 2-chloro-4-iodonicotinic acid (CB Research & Development, Inc., 0.58 g, 2.0 mmol) and 2,4-difluoroaniline (Aldrich, 0.21 mL, 2.0 mmol) in anhydrous DMF (7 mL) was added PyBroP (Novabiochem, 1.4 g, 3.1 mmol) followed by DIPEA (1.1 mL, 6.6 mmol). The mixture was stirred for 63 hours, and then partitioned between chloroform and 10% LiCl (aq). After the aqueous layer was extracted with chloroform, the combined organic layers were washed twice with 10% LiCl (aq), dried over anhydrous MgSO4, and then concentrated in vacuo. Purification of the residue by flash column chromatography (SiO2, eluting with 1:1 hexane/EtOAc) afforded the desired compound (0.43 g, 53%). MS(ESI+) m/z 395 (M+H)+.

後処理

  1. custompartitioned between chloroform and 10% LiCl (aq)
  2. extractionAfter the aqueous layer was extracted with chloroform
  3. washthe combined organic layers were washed twice with 10% LiCl (aq)
  4. dry with materialdried over anhydrous MgSO4
  5. concentrationconcentrated in vacuo
  6. customPurification of the residue
  7. washby flash column chromatography (SiO2, eluting with 1:1 hexane/EtOAc)

出典と根拠

ORDレコード
ord-82b843af914a40afad82a3840811096e
出典データセット
uspto-grants-2009_06
特許番号
US07547782B2

反応ノート

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