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Phosgene → N,N-Dimethyl-2-{N-[N-(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]aminosulfonyl}-4-nitrobenzamide

HRID 840343
ノート
印刷プレビュー

反応式

HRID 840343 の反応式
[NH2:1][C:2]1[N:7]=[C:6]([O:8][CH3:9])[CH:5]=[C:4]([O:10][CH3:11])[N:3]=1.[C:12](Cl)(Cl)=[O:13].C(N(CC)CC)C.[CH3:23][N:24]([CH3:40])[C:25](=[O:39])[C:26]1[CH:31]=[CH:30][C:29]([N+:32]([O-:34])=[O:33])=[CH:28][C:27]=1[S:35]([NH2:38])(=[O:37])=[O:36].[OH-].[K+]>C(OCC)(=O)C>[CH3:23][N:24]([CH3:40])[C:25](=[O:39])[C:26]1[CH:31]=[CH:30][C:29]([N+:32]([O-:34])=[O:33])=[CH:28][C:27]=1[S:35]([NH:38][C:12]([NH:1][C:2]1[N:3]=[C:4]([O:10][CH3:11])[CH:5]=[C:6]([O:8][CH3:9])[N:7]=1)=[O:13])(=[O:36])=[O:37]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 6371Phosgene2 回HCID 8471Triethylamine2 回HCID 14797Potassium HydroxideHCID 1189462-Amino-4,6-dimethoxypyrimidineHCID 22066001N,N-Dimethyl-4-nitro-2-sulfamoylbenzamide

生成物 1

HCID 15335261N,N-Dimethyl-2-{N-[N-(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]aminosulfonyl}-4-nitrobenzamide

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒3 回

反応条件

温度
-10 °C

実験手順

Ethyl acetate (16 ml) and 2-amino-4,6-dimethoxypyrimidine (5.0 g, 32.2 mmol) were introduced and cooled to −10° C. under nitrogen. Phosgene (5.1 g, 51.5 mmol) was passed in at this temperature and a solution of triethylamine (6.5 g, 64.2 mmol) in ethyl acetate (20 ml) was added dropwise in the course of 1 hour. After 1 hour, the reaction was warmed to 20° C. and nitrogen was blown through until it no longer contained phosgene, and then N,N-dimethyl-2-aminosulfonyl-4-nitrobenzamide (8.1 g, 29.6 mmol) was added. The mixture was cooled to −10° C. and a solution of triethylamine (3.3 g, 32.7 mmol) in ethyl acetate (15 ml) was added dropwise in the course of 60 minutes, and the mixture was stirred for 30 minutes and warmed to room temperature. Potassium hydroxide solution (1.0M, 100 ml) was then added, the phases were separated and the aqueous phase was extracted with ethyl acetate. The aqueous phase was adjusted to pH=2 using 6M hydrochloric acid, and the product was filtered off, washed with water (2×20 ml) and dried. Yield: 10.28 g, 72.6% of theory.

後処理

  1. temperaturethe reaction was warmed to 20° C.
  2. temperatureThe mixture was cooled to −10° C.
  3. temperaturewarmed to room temperature
  4. customthe phases were separated
  5. extractionthe aqueous phase was extracted with ethyl acetate
  6. filtrationthe product was filtered off
  7. washwashed with water (2×20 ml)
  8. customdried

出典と根拠

ORDレコード
ord-4cc32cfe09164902a483753d9968b94c
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06365739B1

反応ノート

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