Hydrochloric Acid → 2-((1R,2R)-1-amino-2-hydroxypropyl)-5-(3-(cyclopropylamino)-6-fluoro-2-methylquinoxalin-5-yl)-1H-pyrrole-3-carboxylic acid

HRID 1056231ノート

反応式

HRID 1056231 の反応式
[CH:1]1([NH:4][C:5]2[C:6]([CH3:28])=[N:7][C:8]3[C:13]([N:14]=2)=[C:12]([C:15]2[NH:19][C:18]4[C@H:20]([C@H:24]([OH:26])[CH3:25])[NH:21][C:22](=[O:23])[C:17]=4[CH:16]=2)[C:11]([F:27])=[CH:10][CH:9]=3)[CH2:3][CH2:2]1.[Li+].[OH-:30].Cl>O1CCOCC1.O>[NH2:21][C@H:20]([C:18]1[NH:19][C:15]([C:12]2[C:11]([F:27])=[CH:10][CH:9]=[C:8]3[C:13]=2[N:14]=[C:5]([NH:4][CH:1]2[CH2:2][CH2:3]2)[C:6]([CH3:28])=[N:7]3)=[CH:16][C:17]=1[C:22]([OH:23])=[O:30])[C@H:24]([OH:26])[CH3:25]

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 89783316(6R)-2-(3-(cyclopropylamino)-6-fluoro-2-methyl-5-quinoxalinyl)-6-((1R)-1-hydroxyethyl)-5,6-dihydropyrrolo[3,4-b]pyrrol-4(1H)-one

生成物 1

HCID 897937832-((1R,2R)-1-amino-2-hydroxypropyl)-5-(3-(cyclopropylamino)-6-fluoro-2-methylquinoxalin-5-yl)-1H-pyrrole-3-carboxylic acid

試薬・触媒・溶媒 2

HCID 962Water触媒HCID 312751,4-Dioxane溶媒3 回

反応条件

温度
100 °C

実験手順

The yellow foam (352b) (184.5 mg) in 1,4-dioxane (6.0 mL) was treated with 1.0 M aq. LiOH (3.0 mL, 3.0 mmol). The mixture was heated at 100° C. for 16 h. The mixture was lyophilized to give a yellow solid containing m/z (ESI, +ve) 614.1 (M+H). The yellow solid was dissolved in 1 mL of dioxane and treated with a solution of 4 M HCl in 1,4-dioxane (5 mL) with a few drops of water added to aid solubility. The mixture was stirred at RT for 4 h, after which time bis-deprotection was observed by LC-MS. The mixture was lyophilized to give 2-((1R,2R)-1-amino-2-hydroxypropyl)-5-(3-(cyclopropylamino)-6-fluoro-2-methylquinoxalin-5-yl)-1H-pyrrole-3-carboxylic acid (352c) as a brown solid. A solution of the 2-((1R,2R)-1-amino-2-hydroxypropyl)-5-(3-(cyclopropylamino)-6-fluoro-2-methylquinoxalin-5-yl)-1H-pyrrole-3-carboxylic acid (352c) in DMF (3.0 mL) was treated with TEA (0.20 mL, 1.44 mmol) followed by PyBOP (NovaBiochem) (300 mg, 0.57 mmol). The mixture was stirred at RT for 16 h. The mixture was concentrated, dissolved in DMSO (5.0 mL), and purified by preparative HPLC (Gradient: 10-100% MeCN in H2O, modified with 0.1% TFA) to give (R)-2-(3-(cyclopropylamino)-6-fluoro-2-methylquinoxalin-5-yl)-6-((R)-1-hydroxyethyl)-5,6-dihydropyrrolo[3,4-b]pyrrol-4(1H)-one bis(2,2,2-trifluoroacetate) (352) (54 mg, 0.089 mmol) as a red gum. LC-MS m/z 382.1, [M+H]+; 19F NMR (DMSO-d6; 376 MHz): δ −108.08 (s, 1F), −74.95 (s, 6F).

後処理

  1. customto give a yellow solid
  2. additioncontaining m/z (ESI, +ve) 614.1 (M+H)
  3. additionadded

出典と根拠

ORDレコード
ord-45dcb8a5c7fe4b2480929524a76cce48
出典データセット
uspto-grants-2016_07
特許番号
US09394297B2

反応ノート

読み込み中…