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Pyridine → N-(6-Bromo-1-methyl-1H-indazol-4-yl)-2-(chloromethyl)-1,3-thiazole-4-carboxamide

HRID 1695740
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HRID 1695740 반응식
[Br:1][C:2]1[CH:3]=[C:4]([NH2:12])[C:5]2[CH:6]=[N:7][N:8]([CH3:11])[C:9]=2[CH:10]=1.N1C=CC=CC=1.Cl[CH2:20][C:21]1[N:22]=[C:23]([C:26]([Cl:28])=O)[S:24][CH:25]=1.C(=O)(O)[O-:30].[Na+]>C(Cl)Cl.O>[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][N:8]2[CH3:11])=[C:4]([NH:12][C:20]([C:21]2[N:22]=[C:23]([CH2:26][Cl:28])[S:24][CH:25]=2)=[O:30])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 1049PyridineHCID 516892Sodium BicarbonateHCID 106079144-(chloromethyl)-1,3-thiazole-2-carbonyl ChlorideHCID 582557716-Bromo-1-methyl-1h-indazol-4-amine

생성물 1

HCID 58255850N-(6-Bromo-1-methyl-1H-indazol-4-yl)-2-(chloromethyl)-1,3-thiazole-4-carboxamide

시약·촉매·용매 2

HCID 962
Water
용매
HCID 6344Dichloromethane용매3회

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온도
0 °C

실험 절차

6-Bromo-1-methyl-1H-indazol-4-amine (1 g, 4.42 mmol) was dissolved in DCM (DCM) (10 ml) and pyridine (0.429 ml, 5.31 mmol) added. The mixture was cooled to 0° C. in an ice-water bath and 4-(chloromethyl)-1,3-thiazole-2-carbonyl chloride (0.867 g, 4.42 mmol) in DCM (10 ml) was added portionwise over 5 mins. The mixture was stirred for 2 hours and allowed to warm to room temperature. Saturated sodium bicarbonate solution (15 ml) was added and the mixture stirred vigorously for 10 mins. The mixture was diluted with water (50 ml) and DCM (50 ml), but a precipitate was still present. This was collected by filtration, washed with DCM and air dried to afford the title compound as a yellow/brown solid (860 mg).

후처리

  1. temperatureto warm to room temperature
  2. stirringthe mixture stirred vigorously for 10 mins
  3. filtrationThis was collected by filtration
  4. washwashed with DCM and air
  5. customdried

출처 및 근거

ORD 기록
ord-a1b85bcd996b4b8b90c3117eef7f7687
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163743B2

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