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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1,3-Dioxolane-2-methanamine, N-methyl- → N-(2-trifluoromethyl-1,3,4-thiadiazol-5-yl)-N'-(1,3-dioxolan-2-ylmethyl)-N'-methylurea

HRID 1605796
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HRID 1605796 반응식
[F:1][C:2]([F:12])([F:11])[C:3]1[S:4][C:5]([N:8]=[C:9]=[O:10])=[N:6][N:7]=1.[O:13]1[CH2:17][CH2:16][O:15][CH:14]1[CH2:18][NH:19][CH3:20]>C1C=CC=CC=1>[F:12][C:2]([F:11])([F:1])[C:3]1[S:4][C:5]([NH:8][C:9]([N:19]([CH2:18][CH:14]2[O:15][CH2:16][CH2:17][O:13]2)[CH3:20])=[O:10])=[N:6][N:7]=1
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참가 물질

4

반응물 2

HCID 5417541,3-Dioxolane-2-methanamine, N-methyl-HCID 131418952-Isocyanato-5-(trifluoromethyl)-1,3,4-thiadiazole

생성물 1

HCID 21544990N-(2-trifluoromethyl-1,3,4-thiadiazol-5-yl)-N'-(1,3-dioxolan-2-ylmethyl)-N'-methylurea

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

2-Trifluoromethyl-1,3,4-thiadiazol-5-yl isocyanate dimer (3.1 grams) was added to a solution of N-(1,3-dioxolan-2-ylmethyl)-N-methylamine (2grams) in benzene (10 ml) contained in a glass reaction vessel equipped with a mechanical stirrer and thermometer. The mixture was heated on a steam bath for a period of about 1 hour. The mixture was then stripped of solvent under reduced pressure to yield a solid residue. The residue was recrystallized from an ether-pentane mixture to yield the desired product N-(2-trifluoromethyl-1,3,4-thiadiazol-5-yl)-N'-(1,3-dioxolan-2-ylmethyl)-N'-methylurea having a melting point of 114° to 115°C.

후처리

  1. customcontained in a glass reaction vessel
  2. customequipped with a mechanical stirrer
  3. temperatureThe mixture was heated on a steam bath for a period of about 1 hour
  4. customto yield a solid residue
  5. customThe residue was recrystallized from an ether-pentane mixture

출처 및 근거

ORD 기록
ord-f797ef40af9d4d5a8eb4bce37f37af52
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03951640

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