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Chlorosuccinimide → 5-Chloro-2-formylamino-4-(4-pyridylthiomethyl)thiazole

HRID 1656968
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HRID 1656968 반응식
[CH:1]([NH:3][C:4]1[S:5][CH:6]=[C:7]([CH2:9][S:10][C:11]2[CH:16]=[CH:15][N:14]=[CH:13][CH:12]=2)[N:8]=1)=[O:2].[Cl:17]N1C(=O)CCC1=O>C(O)(=O)C>[Cl:17][C:6]1[S:5][C:4]([NH:3][CH:1]=[O:2])=[N:8][C:7]=1[CH2:9][S:10][C:11]1[CH:16]=[CH:15][N:14]=[CH:13][CH:12]=1
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 15729168HCID 15729168, 화합물

생성물 1

HCID 157291695-Chloro-2-formylamino-4-(4-pyridylthiomethyl)thiazole수율 46.8%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 2-formylamino-4-(4-pyridylthiomethyl)thiazole (1.6 g) and N-chlorosuccinimide (1.5 g) in acetic acid (25 ml) was heated at 40°-50° C. for 5 hours with stirring and then the mixture was allowed to stand at room temperature for 16 hours. The reaction mixture was concentrated under reduced pressure and the residue was triturated with aqueous sodium bicarbonate. The precipitates were collected by filtration washed with water and dried in vacuo to give 5-chloro-2-formylamino-4-(4-pyridylthiomethyl)thiazole (0.85 g, yield: 46.8%). mp: 200°-203° C. (dec.) IR (Nujol): 1680, 1665, 1587, 1300 cm-1

후처리

  1. temperaturewas heated at 40°-50° C. for 5 hours
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customthe residue was triturated with aqueous sodium bicarbonate
  4. filtrationThe precipitates were collected by filtration
  5. washwashed with water
  6. customdried in vacuo

출처 및 근거

ORD 기록
ord-f074c0db8c9941cc8392e977537fb9a9
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05256675

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