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Isopropylamine → HCID 59208314, 화합물

HRID 2061871
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인쇄 미리보기

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HRID 2061871 반응식
[Br:1][C:2]1[C:3]([C:16]2[S:17][CH:18]=[C:19]([C:21]([F:24])([F:23])[F:22])[N:20]=2)=[CH:4][C:5]([NH:8][C:9](=[O:15])OC(C)(C)C)=[N:6][CH:7]=1.[CH:25]([NH2:28])([CH3:27])[CH3:26]>C(#N)C>[Br:1][C:2]1[C:3]([C:16]2[S:17][CH:18]=[C:19]([C:21]([F:22])([F:23])[F:24])[N:20]=2)=[CH:4][C:5]([NH:8][C:9]([NH:28][CH:25]([CH3:27])[CH3:26])=[O:15])=[N:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6363IsopropylamineHCID 67028693HCID 67028693, 화합물2회

생성물 1

HCID 59208314HCID 59208314, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
130 °C

실험 절차

A mixture of tert-butyl 5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-ylcarbamate (Intermediate 87, 25 g, 59 mmol), isopropyl amine (250 mL) and acetonitrile (100 mL) was heated at 130° C. in a Parr Bomb apparatus for 50 h (˜150 PSI). The reaction mixture was cooled to room temperature and the reaction filtered through Celite, and the filtrate was washed with tetrahydrofuran (˜300 mL). The solvents were evaporated and the residue was triturated with methanol (200 mL), filtered and the solid was dried to give 14.6 g of product.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. filtrationthe reaction filtered through Celite
  3. washthe filtrate was washed with tetrahydrofuran (˜300 mL)
  4. customThe solvents were evaporated
  5. customthe residue was triturated with methanol (200 mL)
  6. filtrationfiltered
  7. customthe solid was dried

출처 및 근거

ORD 기록
ord-08e81bdbe5d44de1afb809ee04029684
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08283361B2

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