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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 22929860, 화합물 → HCID 22929965, 화합물

HRID 1295932
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인쇄 미리보기

반응식

HRID 1295932 반응식
[CH3:1][NH:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([C:10]#[N:11])[C:7]([CH2:12][N:13]=[N+]=[N-])=[CH:6][C:5]=1[O:16][CH2:17][CH3:18]>O1CCCC1.N.C(P(CC)CC)C>[CH3:1][NH:2][C:3]([C:4]1[CH:9]=[C:8]2[C:7](=[CH:6][C:5]=1[O:16][CH2:17][CH3:18])[CH2:12][N:13]=[C:10]2[NH2:11])=[O:19]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 22929860HCID 22929860, 화합물

생성물 1

HCID 22929965HCID 22929965, 화합물수율 43.6%

시약·촉매·용매 3

HCID 222Ammonia용매HCID 8028Tetrahydrofuran용매HCID 27365Triethylphosphine용매

반응 조건

온도
50 °C

실험 절차

After dissolving N1-methyl-4-(azidomethyl)-5-cyano-2-ethoxybenzamide (931 mg) in tetrahydrofuran (10 ml), 28% aqueous ammonia (2 ml) and triethylphosphine (0.4 ml) were added in that order. The mixture was stirred at 50° C. for 15 minutes. The precipitated crystals were filtered off, washed with tetrahydrofuran, water and ethyl acetate in that order and dried to yield the title compound (365 mg).

후처리

  1. additionwere added in that order
  2. filtrationThe precipitated crystals were filtered off
  3. washwashed with tetrahydrofuran, water and ethyl acetate in that order
  4. customdried

출처 및 근거

ORD 기록
ord-3e5ef1b9426a41e2ad7c3258811dfae9
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07244730B2

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