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Hydrochloric Acid → HCID 178483273, 화합물

HRID 1982228
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HRID 1982228 반응식
[NH2:1][C:2]1[C:6]([NH:7][CH2:8][CH2:9][S:10][CH2:11][C:12]2[CH:16]=[C:15]([CH2:17][N:18]([CH3:20])[CH3:19])[S:14][CH:13]=2)=[N:5]S(=O)[N:3]=1.[ClH:22]>CO>[ClH:22].[ClH:22].[ClH:22].[CH3:20][N:18]([CH2:17][C:15]1[S:14][CH:13]=[C:12]([CH2:11][S:10][CH2:9][CH2:8][NH:7][C:6](=[NH:5])[C:2](=[NH:1])[NH2:3])[CH:16]=1)[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 23312529HCID 23312529, 화합물

생성물 1

HCID 178483273HCID 178483273, 화합물수율 80%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A suspension of 3-amino-4-{2-[(5-dimethylaminomethyl-3-thienyl)methylthio]ethylamino}-1,2,5-thiadiazole 1-oxide (7.8 g; 22.6 mmoles) [prepared according to published United Kingdom Patent Application No. 2,067,987] in 150 ml of methanol was treated with 15.0 ml of concentrated HCl. After stirring at ambient temperature for 3 hours, the solution was concentrated and the residue triturated with 1-propanol, filtered and dried to give 7.38 g (80%) of product. A sample was recrystallized from methanol-acetone to give the title compound, mp 190°-205° C. (dec.).

후처리

  1. concentrationthe solution was concentrated
  2. customthe residue triturated with 1-propanol
  3. filtrationfiltered
  4. customdried

출처 및 근거

ORD 기록
ord-8f3425948e1c4744bb25ba9c633a4187
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04595758

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