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Diisopropylethylamine → HCID 68485337、化合物

HRID 1875089
ノート
印刷プレビュー

反応式

HRID 1875089 の反応式
CCN(C(C)C)C(C)C.[NH2:10][CH2:11][C:12]1[C:13]([F:29])=[C:14]([O:19][C:20]2[CH:21]=[C:22]([CH:25]=[C:26]([Cl:28])[CH:27]=2)[C:23]#[N:24])[C:15]([Cl:18])=[CH:16][CH:17]=1.[CH3:30][C:31]1[NH:35][C:34](=[O:36])[NH:33][C:32]=1[C:37](O)=[O:38].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(=O)(O)[O-].[Na+]>CN(C=O)C.C(OCC)(=O)C>[Cl:18][C:15]1[CH:16]=[CH:17][C:12]([CH2:11][NH:10][C:37]([C:32]2[NH:33][C:34](=[O:36])[NH:35][C:31]=2[CH3:30])=[O:38])=[C:13]([F:29])[C:14]=1[O:19][C:20]1[CH:21]=[C:22]([C:23]#[N:24])[CH:25]=[C:26]([Cl:28])[CH:27]=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 5

HCID 81531DiisopropylethylamineHCID 516892Sodium BicarbonateHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 135585675-methyl-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acidHCID 594513923-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile

生成物 1

HCID 68485337
HCID 68485337、化合物
収率 95.7%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

DIPEA (0.20 mL, 1.16 mmol) was added to a mixture of 3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.15 g, 0.48 mmol), 5-methyl-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid (0.080 g, 0.58 mmol) and HATU (0.24 g, 0.63 mmol) in DMF (3 mL). The yellow solution was stirred at RT under nitrogen for 24 h then ethyl acetate (50 mL) and saturated sodium bicarbonate solution (100 mL) was added. The organic layer was separated, washed with saturated sodium bicarbonate solution (50 mL), water (50 mL), brine (50 mL) and dried over MgSO4. The mixture was filtered and the solvent was removed under vacuum. The crude material was purified by Reverse Phase HPLC (MeCN/water+0.1% TFA) to give the title compound (0.20 g, 10%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 10.42 (br. s., 1H), 9.75 (br. s., 1H), 7.74-7.95 (m, 2H), 7.42-7.57 (m, 3H), 7.37 (t, 1H), 4.44 (d, 2H), 2.20 (s, 3H). LCMS m/z 437.0 (M+H).

後処理

  1. customThe organic layer was separated
  2. washwashed with saturated sodium bicarbonate solution (50 mL), water (50 mL), brine (50 mL)
  3. dry with materialdried over MgSO4
  4. filtrationThe mixture was filtered
  5. customthe solvent was removed under vacuum
  6. customThe crude material was purified by Reverse Phase HPLC (MeCN/water+0.1% TFA)

出典と根拠

ORDレコード
ord-cb378c72989e4821a19e2ab29970c94c
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08304419B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート