2-Bromopyrimidine → (S)-tert-Butyl 2-(5-(4'-(2-((S)-1-((S)-3-methyl-2-(pyrimidin-2-ylamino)butanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate

HRID 588956

反応式

HRID 588956 の反応式
[NH2:1][C@@H:2]([CH:44]([CH3:46])[CH3:45])[C:3]([N:5]1[CH2:9][CH2:8][CH2:7][C@H:6]1[C:10]1[NH:11][C:12]([C:15]2[CH:20]=[CH:19][C:18]([C:21]3[CH:26]=[CH:25][C:24]([C:27]4[NH:31][C:30]([C@@H:32]5[CH2:36][CH2:35][CH2:34][N:33]5[C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])=[N:29][CH:28]=4)=[CH:23][CH:22]=3)=[CH:17][CH:16]=2)=[CH:13][N:14]=1)=[O:4].Br[C:48]1[N:53]=[CH:52][CH:51]=[CH:50][N:49]=1.CCN(C(C)C)C(C)C>C1(C)C=CC=CC=1.CS(C)=O>[CH3:45][CH:44]([CH3:46])[C@H:2]([NH:1][C:48]1[N:53]=[CH:52][CH:51]=[CH:50][N:49]=1)[C:3]([N:5]1[CH2:9][CH2:8][CH2:7][C@H:6]1[C:10]1[NH:11][C:12]([C:15]2[CH:20]=[CH:19][C:18]([C:21]3[CH:22]=[CH:23][C:24]([C:27]4[NH:31][C:30]([C@@H:32]5[CH2:36][CH2:35][CH2:34][N:33]5[C:37]([O:39][C:40]([CH3:41])([CH3:43])[CH3:42])=[O:38])=[N:29][CH:28]=4)=[CH:25][CH:26]=3)=[CH:17][CH:16]=2)=[CH:13][N:14]=1)=[O:4]

参加物

5

反応物 3

HCID 783452-BromopyrimidineHCID 81531DiisopropylethylamineHCID 59166546(S)-tert-butyl 2-(5-(4'-(2-((S)-1-((s)-2-amino-3-methylbutanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate

生成物 1

HCID 59166544(S)-tert-Butyl 2-(5-(4'-(2-((S)-1-((S)-3-methyl-2-(pyrimidin-2-ylamino)butanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate収率 110.8%

試薬・触媒・溶媒 1

HCID 22340214Dimethylsulfoxide toluene溶媒

反応条件

温度
90 °C

実験手順

A mixture of (S)-tert-butyl 2-(5-(4′-(2-((S)-1-((S)-2-amino-3-methylbutanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (cj-2) (0.45 g, 0.72 mmol), 2-bromopyrimidine (0.37 g, 2.34 mmol) and iPr2NEt (0.20 mL, 1.18 mmol) in toluene-DMSO (4:1, 5 mL) was heated at 90° C. overnight. The volatiles were removed in vacuo and the residue was purified by preparative HPLC (YMC Pack C-18, 30×100 mm/MeCN—H2O-TFA). The title compound (0.56 g, 74%), as its TFA salt, was obtained as a yellow-orange glass.

後処理

  1. customThe volatiles were removed in vacuo
  2. customthe residue was purified by preparative HPLC (YMC Pack C-18, 30×100 mm/MeCN—H2O-TFA)

出典と根拠

ORDレコード
ord-91a6896058264bae97988c24b63d0ea2
出典データセット
uspto-grants-2016_01
特許番号
US09227961B2

関連ノート

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