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Hydrochloric Acid → HCID 66623754, 화합물

HRID 1684912
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인쇄 미리보기

반응식

HRID 1684912 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]3[CH:15]=[CH:14][C:13]([B:16]4[O:20]C(C)(C)C(C)(C)[O:17]4)=[CH:12][N:11]3[CH:25]=2)=[CH:4][CH:3]=1.Cl>CC(C)=O.O>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[N:9]=[C:10]3[CH:15]=[CH:14][C:13]([B:16]([OH:20])[OH:17])=[CH:12][N:11]3[CH:25]=2)=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 44232240HCID 44232240, 화합물

생성물 1

HCID 66623754HCID 66623754, 화합물수율 138.4%

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매

실험 절차

7.93 g of 2-(4-chlorophenyl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine are dissolved in 200 ml of acetone and 100 ml of water; 223 ml of 1N hydrochloric acid are added thereto, dropwise there with stirring, and the mixture is stirred at ambient temperature for 16 h. The reaction mixture is subsequently concentrated under reduced pressure. 4.78 g of compound are obtained, which compound is used as is in the following stages.

후처리

  1. stirringthe mixture is stirred at ambient temperature for 16 h
  2. concentrationThe reaction mixture is subsequently concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-0207dd44f5d540b98e2a80c1a1e244c9
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08148370B2

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