홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Dibutyltin oxide → HCID 178509305, 화합물

HRID 1371547
노트
인쇄 미리보기

반응식

HRID 1371547 반응식
[NH2:1][C:2]1[C:3]([C:7]#[N:8])=[N:4][O:5][N:6]=1.C[Si]([N:13]=[N+:14]=[N-:15])(C)C.C([Sn](=O)CCCC)CCC>C1(C)C=CC=CC=1>[NH:13]1[C:7]([C:3]2[C:2]([NH2:1])=[N:6][O:5][N:4]=2)=[N:8][N:15]=[N:14]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 61221Dibutyltin oxideHCID 78378AzidotrimethylsilaneHCID 12527694-Amino-1,2,5-oxadiazole-3-carbonitrile

생성물 1

HCID 178509305HCID 178509305, 화합물수율 88.5%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of 4-amino-furazan-3-carbonitrile (0.10 g, 0.90 mmol) and trimethylsilyl azide (0.21 g, 1.82 mmol) in toluene (10 mL) was added dibutyl tin oxide (0.227 g, 0.91 mmol) and the mixture was heated for 20 hours at 130° C. until complete consumption of nitrile was observed by LC-MS. The reaction mixture was allowed to cool to ambient temperature and concentrated in vacuo. The residue was dissolved in methanol and partitioned between ethyl acetate and 10% sodium bicarbonate solution and the organic portion was washed with a further portion of 10% sodium bicarbonate solution. The combined aqueous extracts were acidified to pH 2 with 10% HCl solution and re-extracted into ethyl acetate (2×30 mL). The combined organics were dried over MgSO4, filtered and concentrated in vacuo to yield 4-(1H-tetrazol-5-yl)-furazan-3-ylamine as a white solid (0.122 g, 87%).

후처리

  1. concentrationconcentrated in vacuo
  2. dissolutionThe residue was dissolved in methanol
  3. custompartitioned between ethyl acetate and 10% sodium bicarbonate solution
  4. washthe organic portion was washed with a further portion of 10% sodium bicarbonate solution
  5. extractionre-extracted into ethyl acetate (2×30 mL)
  6. dry with materialThe combined organics were dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-c4b11abf6770440298373bc1b0762931
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07157476B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트