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Isopropylamine → HCID 3055551, 화합물

HRID 444306
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HRID 444306 반응식
[CH3:1][C:2]1[S:3][C:4]([CH:7]=[CH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[O:15][CH2:16][CH:17]2[O:19][CH2:18]2)=[N:5][N:6]=1.[CH:20]([NH2:23])([CH3:22])[CH3:21]>C(O)(C)C>[CH3:1][C:2]1[S:3][C:4]([CH:7]=[CH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[O:15][CH2:16][CH:17]([OH:19])[CH2:18][NH:23][CH:20]([CH3:22])[CH3:21])=[N:5][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6363IsopropylamineHCID 53934759HCID 53934759, 화합물

생성물 1

HCID 3055551HCID 3055551, 화합물

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

7 g (0.025 mole) of 2-methyl-5-[2-(2,3-epoxypropoxy)-styryl]-1,3,4-thiadiazole and 2.9 g (0.05 mole) of isopropylamine are mixed in 100 ml of isopropanol and the mixture is refluxed for 7 hours. On cooling, a precipitate forms; this is recrystallized from toluene, together with the solid residue obtained from concentrating the mother liquor. 5.1 g (61% of theory), melting point 156°-157°.

후처리

  1. temperaturethe mixture is refluxed for 7 hours
  • temperatureOn cooling
  • customthis is recrystallized from toluene, together with the solid residue
  • customobtained
  • concentrationfrom concentrating the mother liquor
  • 출처 및 근거

    ORD 기록
    ord-71791f864f4e4e64aaf1a017235f0597
    출처 데이터셋
    uspto-grants-1981_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04263430

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