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Acetic Acid → HCID 178475878, 화합물

HRID 704505
노트
인쇄 미리보기

반응식

HRID 704505 반응식
[OH:1][C:2]1[N:7]2[N:8]=[C:9]([CH3:11])[N:10]=[C:6]2[N:5]=[C:4]([CH2:12][OH:13])[CH:3]=1.CN(C=O)C.[C:19](O)(=[O:21])[CH3:20].C1(C)C=CC(S(O)(=O)=O)=CC=1>CCOCC.C(O)(C)C>[C:19]([O:13][CH2:12][C:4]1[CH:3]=[C:2]([OH:1])[N:7]2[N:8]=[C:9]([CH3:11])[N:10]=[C:6]2[N:5]=1)(=[O:21])[CH3:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 6101p-Toluenesulfonic acidHCID 6228DimethylformamideHCID 178432391HCID 178432391, 화합물

생성물 1

HCID 178475878HCID 178475878, 화합물

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 3776

반응 조건

온도
50 °C

실험 절차

A mixture of 33.06 g of 7-hydroxy-5-hydroxymethyl-2-methyl-s-triazolo[1,5-a]pyrimidine, 500 ml of DMF, 86 ml of anhydrous acetic acid and 1.5 g of p-toluenesulfonic acid was stirred in a bath at 50 ° C. for 6 hours. To an oily isopropanol to dissolve therein, and the solution was dropwise in 4 liters of ether. Precipitates were collected by filtration and dried to obtain 38.08 g of the compound.

후처리

  1. customPrecipitates
  2. filtrationwere collected by filtration
  3. customdried

출처 및 근거

ORD 기록
ord-b08ce1cfa1334cc4946ef42ab590d8bf
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04987129

반응 노트

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
Isopropanol
용매