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Isopropylamine → [2-(4-Fluorophenyl)-2-methylpropyl]{3-[(methylethyl)amino](1,2,4-thiadiazol-5-yl)}amine

HRID 409350
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HRID 409350 반응식
Cl[C:2]1[N:6]=[C:5]([NH:7][CH2:8][C:9]([C:12]2[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=2)([CH3:11])[CH3:10])[S:4][N:3]=1.[CH:19]([NH2:22])([CH3:21])[CH3:20]>>[F:18][C:15]1[CH:16]=[CH:17][C:12]([C:9]([CH3:11])([CH3:10])[CH2:8][NH:7][C:5]2[S:4][N:3]=[C:2]([NH:22][CH:19]([CH3:21])[CH3:20])[N:6]=2)=[CH:13][CH:14]=1
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참가 물질

3

반응물 2

HCID 6363IsopropylamineHCID 709750603-Chloro-N-(2-(4-fluorophenyl)-2-methylpropyl)-1,2,4-thiadiazol-5-amine

생성물 1

HCID 70977343[2-(4-Fluorophenyl)-2-methylpropyl]{3-[(methylethyl)amino](1,2,4-thiadiazol-5-yl)}amine

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온도
110 °C

실험 절차

3-Chloro-N-(2-(4-fluorophenyl)-2-methylpropyl)-1,2,4-thiadiazol-5-amine (50 mg, 0.18 mmol, 1.0 equiv) and i-PrNH2 (0.5 mL, 5.8 mmol) were loaded into a microwave vial, and the resulting mixture was heated to 110° C. for 30 minutes. The reaction mixture was then concentrated in vacuo. Purification by silica gel (20-30% EtOAc/Hexanes) provided the title compound as an off white solid (55 mg, 99%). m/z=309.1 [M+H]+.

후처리

  1. concentrationThe reaction mixture was then concentrated in vacuo
  2. customPurification by silica gel (20-30% EtOAc/Hexanes)

출처 및 근거

ORD 기록
ord-f42e3f5f25e843498f42b40181412fd4
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08759380B2

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