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Dimethyl Sulfoxide → HCID 13983453, 화합물

HRID 580457
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HRID 580457 반응식
[NH2:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[N:5][C:6](Cl)=[CH:7][CH:8]=2)[N:3]=1.[CH3:13][N:14]([CH3:19])[CH2:15][CH2:16][CH2:17][SH:18].[OH-].[K+].CS(C)=O>C(OCC)C.O>[NH2:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[N:5][C:6]([S:18][CH2:17][CH2:16][CH2:15][N:14]([CH3:19])[CH3:13])=[CH:7][CH:8]=2)[N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 679Dimethyl SulfoxideHCID 14797Potassium HydroxideHCID 851997-Chloro-1,8-naphthyridin-2-amineHCID 30169983-(Dimethylamino)-1-propanethiol

생성물 1

HCID 13983453HCID 13983453, 화합물수율 77%

시약·촉매·용매 2

HCID 962Water용매
HCID 3283
Diethyl Ether
용매

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온도
90 °C

실험 절차

A mixture composed of 2-amino-7-chloro-1,8-naphthyridine (8 g), 3-dimethylaminopropanethiol (11.4 g), potassium hydroxide pellets (85% pure; 6.26 g) and dimethyl sulphoxide (87 cc) is heated to 90° C. for 3 hours 30 minutes. The reaction mixture is then poured into water (1500 cc) and extracted with methylene chloride (5×400 cc). The organic extracts are combined and washed with distilled water (400 cc), dried over magnesium sulphate and concentrated to dryness at 40° C. under reduced pressure (4 kPa). The residue obtained is treated with ethyl ether (100 cc). The insoluble product is separated by filtration, washed with ethyl ether (10 cc) and dried at 40° C. under reduced pressure (0.07 kPa). 2-Amino-7-(3-dimethylaminopropylthio)-1,8-naphthyridine (9 g), m.p. 164° C., is obtained.

후처리

  1. extractionextracted with methylene chloride (5×400 cc)
  2. washwashed with distilled water (400 cc)
  3. dry with materialdried over magnesium sulphate
  4. concentrationconcentrated to dryness at 40° C. under reduced pressure (4 kPa)
  5. customThe residue obtained
  6. customThe insoluble product is separated by filtration
  7. washwashed with ethyl ether (10 cc)
  8. customdried at 40° C. under reduced pressure (0.07 kPa)

출처 및 근거

ORD 기록
ord-77a231e5c32c46cca405cb6342534dc7
출처 데이터셋
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04753933

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