Triethylamine → 5-[5-Bromo-4-(1-ethyl-2-oxo-propylsulfanyl)-pyrimidin-2-ylamino]-pyridine-2-sulfonic acid amide

HRID 1182061

반응식

HRID 1182061 반응식
[Br:1][C:2]1[C:3](Cl)=[N:4][C:5]([NH:8][C:9]2[CH:10]=[CH:11][C:12]([S:15]([NH2:18])(=[O:17])=[O:16])=[N:13][CH:14]=2)=[N:6][CH:7]=1.[SH:20][CH:21]([CH2:25][CH3:26])[C:22](=[O:24])[CH3:23].C(N(CC)CC)C>CN(C=O)C>[Br:1][C:2]1[C:3]([S:20][CH:21]([CH2:25][CH3:26])[C:22](=[O:24])[CH3:23])=[N:4][C:5]([NH:8][C:9]2[CH:10]=[CH:11][C:12]([S:15]([NH2:18])(=[O:17])=[O:16])=[N:13][CH:14]=2)=[N:6][CH:7]=1

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 622373-Mercapto-2-pentanoneHCID 589818655-(5-bromo-4-chloro-pyrimidin-2-ylamino)-pyridine-2-sulfonic Acid Amide

생성물 1

HCID 589818355-[5-Bromo-4-(1-ethyl-2-oxo-propylsulfanyl)-pyrimidin-2-ylamino]-pyridine-2-sulfonic acid amide

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
50 °C

실험 절차

73 mg (0.2 mmol) of 5-(5-bromo-4-chloro-pyrimidin-2-ylamino)-pyridine-2-sulfonic acid amide and 32 mg (0.27 mmol) of 3-mercapto-2-pentanone are dissolved in 4 ml of DMF p.a. After 0.038 ml (0.27 mmol) of triethylamine is added, it is allowed to stir for 2 hours at room temperature and for 3 hours at 50° C. After concentration by evaporation, it is flashed with dichloromethane/MeOH (9:1).

후처리

  1. concentrationAfter concentration
  2. customby evaporation, it

출처 및 근거

ORD 기록
ord-3c4bd87c289f423588e0c9618dde772d
출처 데이터셋
uspto-grants-2007_10
특허 번호
US07288547B2

연결된 노트

불러오는 중…