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Pent-2-yn-1-amine → HCID 178446264, 화합물

HRID 1580647
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HRID 1580647 반응식
[F:1][C:2]([F:22])([F:21])[C:3]1[CH:4]=[CH:5][C:6]2[NH:12][C:11](=S)[CH2:10][N:9]=[C:8]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[C:7]=2[CH:20]=1.[CH2:23]([NH2:28])[C:24]#[C:25][CH2:26][CH3:27]>O1CCCC1>[F:1][C:2]([F:22])([F:21])[C:3]1[CH:4]=[CH:5][C:6]2[N:12]=[C:11]([NH:28][CH2:23][C:24]#[C:25][CH2:26][CH3:27])[CH2:10][N:9]=[C:8]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[C:7]=2[CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11205717Pent-2-yn-1-amineHCID 12947027HCID 12947027, 화합물

생성물 1

HCID 178446264HCID 178446264, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 10.0 g. of 1,3-dihydro-7-(trifluoromethyl)-5-phenyl-2H-1,4-benzodiazepine-2-thione (V), 10.0 g. of 2-pentynylamine, and 150 ml. of dry tetrahydrofuran is stirred under nitrogen at ambient temperature for about 5 hours and then concentrated in vacuo. The residue thus obtained is recrystallized from methanol to give 7-trifluoromethyl-5-phenyl-2-(2-pentynylamino)-3H-1,4-benzodiazepine.

후처리

  1. addition
A mixture of 10.0 g
  • concentrationconcentrated in vacuo
  • customThe residue thus obtained
  • customis recrystallized from methanol
  • 출처 및 근거

    ORD 기록
    ord-2f99ab839b7c43c7b41529024b4d3746
    출처 데이터셋
    uspto-grants-1976_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US03933794

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