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Hydrochloric Acid → HCID 20144964, 화합물

HRID 1906019
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인쇄 미리보기

반응식

HRID 1906019 반응식
[CH3:1][N:2]([C:5]1[S:6][C:7]([C:11]2[N:12]=[C:13]3[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][N:14]3[CH:20]=2)=[C:8]([CH3:10])[N:9]=1)C=O.Cl>C(O)C>[CH3:1][NH:2][C:5]1[S:6][C:7]([C:11]2[N:12]=[C:13]3[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][N:14]3[CH:20]=2)=[C:8]([CH3:10])[N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 20145002HCID 20145002, 화합물

생성물 1

HCID 20144964HCID 20144964, 화합물수율 73.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 2-[2-(N-methylformamido)-4-methylthiazol-5-yl]-7-methylimidazo[1,2-a]pyridine (4.87 g) in ethanol (200 ml) was added 36% hydrochloric acid (2.6 ml) and refluxed for 1.5 hours. The reaction mixture was evaporated. The residue was dissolved in water, and the aqueous mixture was adjusted to pH 8 with saturated potassium carbonate. Extraction with chloroform, and evaporation afforded 2-(2-methylamino-4-methylthiazol-5-yl)-7-methyl-imidazo[1,2-a]pyridine (3.22 g). mp 220°-221° C.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. temperaturerefluxed for 1.5 hours
  2. customThe reaction mixture was evaporated
  3. dissolutionThe residue was dissolved in water
  4. extractionExtraction
  5. customwith chloroform, and evaporation

출처 및 근거

ORD 기록
ord-0d3e78a3f7a341c3adae9331b024c0a3
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04649146

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