Water → (R)-4-{5-[2-Chloro-4-(2-{(2S,4S)-1-[(S)-2-methoxycarbonylamino-2-(tetrahydro-pyran-4-yl)-acetyl]-4-methyl-pyrrolidin-2-yl}-3H-naphtho[1,2-d]imidazol-7-yl)-5-trifluoromethoxy-phenylcarbamoyl]-pyridin-2-yl}-3-methyl-piperazine-1-carboxylic acid tert-butyl ester

HRID 2176470ノート

反応式

HRID 2176470 の反応式
[CH3:1][O:2][C:3](=[O:42])[NH:4][C@@H:5]([CH:36]1[CH2:41][CH2:40][O:39][CH2:38][CH2:37]1)[C:6]([N:8]1[CH2:12][C@@H:11]([CH3:13])[CH2:10][C@H:9]1[C:14]1[NH:15][C:16]2[CH:26]=[CH:25][C:24]3[C:19](=[CH:20][CH:21]=[C:22](B4OC(C)(C)C(C)(C)O4)[CH:23]=3)[C:17]=2[N:18]=1)=[O:7].[C:43]([O:47][C:48]([N:50]1[CH2:55][CH2:54][N:53]([C:56]2[CH:61]=[CH:60][C:59]([C:62](=[O:77])[NH:63][C:64]3[CH:69]=[C:68]([O:70][C:71]([F:74])([F:73])[F:72])[C:67](Br)=[CH:66][C:65]=3[Cl:76])=[CH:58][N:57]=2)[C@H:52]([CH3:78])[CH2:51]1)=[O:49])([CH3:46])([CH3:45])[CH3:44].O.C(=O)([O-])[O-].[K+].[K+]>C1(C)C=CC=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl>[C:43]([O:47][C:48]([N:50]1[CH2:55][CH2:54][N:53]([C:56]2[CH:61]=[CH:60][C:59]([C:62](=[O:77])[NH:63][C:64]3[CH:69]=[C:68]([O:70][C:71]([F:74])([F:73])[F:72])[C:67]([C:22]4[CH:23]=[C:24]5[C:19](=[CH:20][CH:21]=4)[C:17]4[N:18]=[C:14]([C@@H:9]6[CH2:10][C@H:11]([CH3:13])[CH2:12][N:8]6[C:6](=[O:7])[C@@H:5]([NH:4][C:3]([O:2][CH3:1])=[O:42])[CH:36]6[CH2:41][CH2:40][O:39][CH2:38][CH2:37]6)[NH:15][C:16]=4[CH:26]=[CH:25]5)=[CH:66][C:65]=3[Cl:76])=[CH:58][N:57]=2)[C@H:52]([CH3:78])[CH2:51]1)=[O:49])([CH3:46])([CH3:45])[CH3:44]

参加物

7

反応物 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 67494940(R)-4-[5-(4-bromo-2-chloro-5-trifluoromethoxy-phenylcarbamoyl)-pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert-butyl esterHCID 86700557[(S)-2-{(2S,4S)-4-methyl-2-[7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3H-naphth[1,2-d]imidazol-2-yl]-pyrrolidin-1-yl}-2-oxo-1-(tetrahydro-pyran-4-yl)-ethyl]-carbamic acid methyl ester

生成物 1

HCID 86700556(R)-4-{5-[2-Chloro-4-(2-{(2S,4S)-1-[(S)-2-methoxycarbonylamino-2-(tetrahydro-pyran-4-yl)-acetyl]-4-methyl-pyrrolidin-2-yl}-3H-naphtho[1,2-d]imidazol-7-yl)-5-trifluoromethoxy-phenylcarbamoyl]-pyridin-2-yl}-3-methyl-piperazine-1-carboxylic acid tert-butyl ester収率 92.4%

試薬・触媒・溶媒 2

HCID 178418807HCID 178418807、化合物触媒HCID 1140Toluene溶媒

反応条件

温度
90 °C

実験手順

To a mixture of [(S)-2-{(2S,4S)-4-methyl-2-[7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3H-naphth[1,2-d]imidazol-2-yl]-pyrrolidin-1-yl}-2-oxo-1-(tetrahydro-pyran-4-yl)-ethyl]-carbamic acid methyl ester (80 mg, 0.10 mmol; Preparation 23) and (R)-4-[5-(4-bromo-2-chloro-5-trifluoromethoxy-phenylcarbamoyl)-pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert-butyl ester (85 mg, 0.14 mmol) dissolved in toluene (0.92 mL) and water (0.34 mL) was added potassium carbonate (103 mg, 0.75 mmol). The reaction mixture was sparged under nitrogen and Pd(dppf)Cl2 CH2Cl2 (7.0 mg, 0.009 mmol) was added and the reaction mixture was heated to 90° C. overnight, cooled to RT, filtered through a combined pad of Celite® and silica gel and washed with EtOAc. The filtrate was washed with water and brine to produce a brownish colored solid, which was purified by silica chromatography (12 g column, 5-100% EtOAc/hexanes) to produce the title intermediate (89 mg, 60% yield) as a light colored solid. (m/z): [M+H]+ calcd for C48H54ClF3N8O8 963.37 found 963.5.

後処理

  1. customThe reaction mixture was sparged under nitrogen
  2. temperaturecooled to RT
  3. filtrationfiltered through a combined pad of Celite® and silica gel
  4. washwashed with EtOAc
  5. washThe filtrate was washed with water and brine
  6. customto produce a brownish colored solid, which
  7. customwas purified by silica chromatography (12 g column, 5-100% EtOAc/hexanes)

出典と根拠

ORDレコード
ord-02399a29634d4a79b7311c27aee931bb
出典データセット
uspto-grants-2015_06
特許番号
US09066944B2

反応ノート

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