Diisopropylethylamine → HCID 59511750、化合物
反応式
[OH:1][C:2]1[CH:10]=[C:6]([C:7]([OH:9])=O)[C:5]([NH2:11])=[CH:4][CH:3]=1.Cl.CN(C)CCCN=C=NCC.O.ON1C2C=CC=CC=2N=N1.Cl.[NH2:36][CH2:37][C:38]([NH:40][CH:41]([CH3:43])[CH3:42])=[O:39].C(N(CC)C(C)C)(C)C>CN(C=O)C>[NH2:11][C:5]1[CH:4]=[CH:3][C:2]([OH:1])=[CH:10][C:6]=1[C:7]([NH:36][CH2:37][C:38](=[O:39])[NH:40][CH:41]([CH3:43])[CH3:42])=[O:9]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of 5-hydroxyanthranilic acid (7.6 g, 49.3 mmol) in DMF (100 mL) was added 1-[3-dimethylaminopropyl]-3-ethylcarbodiimide hydrochloride (EDC) (10.4 g, 54.2 mmol), 1-hydroxybenzotriazole hydrate (HOBt) (7.3 g, 54.2 mmol), 2-amino-N-isopropyl-acetamide hydrochloride (INTERMEDIATE I.1) (7.5 g, 49.3 mmol) and N,N-diisopropylethylamine (DIEA) (9.50 mL, 7.0 g, 54.2 mmol). The reaction mixture was stirred at room temperature for 24 h, concentrated in vacuo to half of its volume and partitioned between diethyl ether (100 mL) and 1N HCl (aq.) (400 mL). The aqueous layer was extracted with diethyl ether (5×100 mL), and ethyl acetate (5×100 mL). The aqueous layer was then concentrated under high vacuum to dryness. The red residue was dissolved in ethanol (20 mL) followed by addition of dichloromethane (1 L). The resulting brown precipitate was filtered under vacuum and washed with a minimum amount of methanol to give the desired product 2-amino-5-hydroxy-N-(isopropylcarbamoylmethyl)benzamide (INTERMEDIATE I.1) hydrochloride salt as a white solid (5.7 g, 19.8 mmol, 40%).
後処理
- concentrationconcentrated in vacuo to half of its volume
- custompartitioned between diethyl ether (100 mL) and 1N HCl (aq.) (400 mL)
- extractionThe aqueous layer was extracted with diethyl ether (5×100 mL), and ethyl acetate (5×100 mL)
- concentrationThe aqueous layer was then concentrated under high vacuum to dryness
- dissolutionThe red residue was dissolved in ethanol (20 mL)
- additionfollowed by addition of dichloromethane (1 L)
- filtrationThe resulting brown precipitate was filtered under vacuum
- washwashed with a minimum amount of methanol
出典と根拠
- ORDレコード
- ord-6bc693ccf4564e78b5953ca01a6c3032
- 出典データセット
- uspto-grants-2010_10
- 特許番号
- US07807686B2
反応ノート
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