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Water → Tert-butyl 2-hydroxy-3-[(3-nitroquinolin-4-yl)amino]propylcarbamate

HRID 1364016
ノート
印刷プレビュー

反応式

HRID 1364016 の反応式
C(N(CC)CC)C.Cl[C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]=[CH:11][C:10]=1[N+:19]([O-:21])=[O:20].[NH2:22][CH2:23][CH:24]([OH:34])[CH2:25][NH:26][C:27](=[O:33])[O:28][C:29]([CH3:32])([CH3:31])[CH3:30].O>CN(C)C=O.O1CCOCC1>[OH:34][CH:24]([CH2:23][NH:22][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]=[CH:11][C:10]=1[N+:19]([O-:21])=[O:20])[CH2:25][NH:26][C:27](=[O:33])[O:28][C:29]([CH3:31])([CH3:32])[CH3:30]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 8471TriethylamineHCID 10511887tert-butyl N-(3-amino-2-hydroxypropyl)carbamateHCID 112758084-Chloro-3-nitroquinoline

生成物 1

HCID 66958711Tert-butyl 2-hydroxy-3-[(3-nitroquinolin-4-yl)amino]propylcarbamate収率 97.5%

試薬・触媒・溶媒 2

HCID 6228
Dimethylformamide
溶媒
HCID 312751,4-Dioxane溶媒

実験手順

Under a nitrogen atmosphere, triethylamine (72 g, 710 mmol) was added to a solution of 4-chloro-3-nitroquinoline (98.9 g, 474 mmol) in N,N-dimethylformamide (DMF) (1 L). A solution of tert-butyl 3-amino-2-hydroxypropylcarbamate (108.19 g, 569 mmol) in dioxane (800 mL) was slowly added, and the reaction was stirred overnight at ambient temperature and then poured into water (3 L) with continuous stirring. A precipitate formed and was isolated by filtration, washed with water, and dried for three days in a vacuum oven at 65° C. to provide 167.54 g of tert-butyl 2-hydroxy-3-[(3-nitroquinolin-4-yl)amino]propylcarbamate as a bright yellow powder.

後処理

  1. customA precipitate formed
  2. customwas isolated by filtration
  3. washwashed with water
  4. customdried for three days in a vacuum oven at 65° C.

出典と根拠

ORDレコード
ord-e29db353a013467c842504ed08e54198
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07888349B2

反応ノート

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