Hydrochloric Acid → 2-({2-[Bis(carboxymethyl)amino]-5-(4-nitrophenyl)pentyl}({2-[bis(carboxymethyl)amino]ethyl})amino)acetic acid
反応式
C([O:5][C:6](=[O:59])[CH2:7][N:8]([CH2:51][C:52](=[O:58])[O:53]C(C)(C)C)[CH:9]([CH2:39][CH2:40][CH2:41][C:42]1[CH:47]=[CH:46][C:45]([N+:48]([O-:50])=[O:49])=[CH:44][CH:43]=1)[CH2:10][N:11]([CH2:20][CH2:21][N:22]([CH2:31][C:32]([O:34]C(C)(C)C)=[O:33])[CH2:23][C:24](=[O:30])[O:25]C(C)(C)C)[CH2:12][C:13]([O:15]C(C)(C)C)=[O:14])(C)(C)C.Cl.CCOCC>O1CCOCC1>[C:6]([CH2:7][N:8]([CH2:51][C:52]([OH:58])=[O:53])[CH:9]([CH2:39][CH2:40][CH2:41][C:42]1[CH:47]=[CH:46][C:45]([N+:48]([O-:50])=[O:49])=[CH:44][CH:43]=1)[CH2:10][N:11]([CH2:20][CH2:21][N:22]([CH2:31][C:32]([OH:34])=[O:33])[CH2:23][C:24]([OH:30])=[O:25])[CH2:12][C:13]([OH:15])=[O:14])([OH:59])=[O:5]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a flask containing compound 4b (30 mg, 0.0358 mmol) at 0-5° C. was added dropwise 4M HCl (g) in 1,4-dioxane (2 mL) over 10 min. The resulting mixture was gradually warmed to room temperature and continuously stirred for 40 h. Ether (20 mL) was added to the reaction mixture which was then stirred for 10 min. The resulting precipitate was filtered and washed with ether. The solid product was quickly dissolved deionized water. The aqueous solution was concentrated in vacuo to provide 5b (24 mg, 100%) as an off-white solid. 1H NMR (D2O, 300 MHz) δ1.03-1.89 (m, 4H), 2.21-4.32 (m, 20H), 7.27 (s, 2H), 7.97 (s, 2H); 13C NMR (D2O, 300 MHz) δ25.0 (t), 26.3 (t), 34.6 (t), 46.9 (t), 48.7 (t), 52.3 (t), 52.7 (t), 53.6 (t), 54.6 (t), 55.3 (t), 62.4 (d), 123.7 (d), 129.4 (d), 145.9 (s), 150.0 (s), 168.5 (s), 170.5 (s), 172.7 (s).
後処理
- stirringwas then stirred for 10 min
- filtrationThe resulting precipitate was filtered
- washwashed with ether
- dissolutionThe solid product was quickly dissolved
- concentrationThe aqueous solution was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-40e3917446b540a8b96cbedd1384d551
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09446995B2
反応ノート
読み込み中…