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Diisopropylethylamine → 2-Phenyl-pyrimidine-5-carboxylic acid (2-sulfamoyl-ethyl)-amide

HRID 219684
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반응식

HRID 219684 반응식
[C:1]1([C:7]2[N:12]=[CH:11][C:10]([C:13](Cl)=[O:14])=[CH:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:16][CH2:17][CH2:18][S:19]([NH2:22])(=[O:21])=[O:20].C(N(C(C)C)CC)(C)C>C(Cl)Cl>[S:19]([CH2:18][CH2:17][NH:16][C:13]([C:10]1[CH:9]=[N:8][C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[N:12][CH:11]=1)=[O:14])(=[O:21])(=[O:20])[NH2:22]
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참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 101263TaurinamideHCID 106326372-phenylpyrimidine-5-carbonyl Chloride

생성물 1

HCID 166661752-Phenyl-pyrimidine-5-carboxylic acid (2-sulfamoyl-ethyl)-amide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 2-phenyl-pyrimidine-5-carboxylic acid chloride (1.51 mmol) and 2-amino-ethanesulfonic acid amide (1.51 mmol) in DCM (15 mL) is added diisopropylethylamine (4.53 mmol). The mixture is stirred at room temperature overnight. The mixture is concentrated in vacuo. The residue is washed with water and DCM to afford 2-phenyl-pyrimidine-5-carboxylic acid (2-sulfamoyl-ethyl)-amide as a solid. MS: 307 (M+H); 1H NMR (300 MHz, DMSO-d6): δ 3.25 (q, 2H), 3.67 (m, 2H), 6.93 (s, N—H), 7.47-7.60 (m, 3H), 8.36-8.48 (m, 2H), 8.92-9.15 (m, N—H), 9.16-9.36 (m, 2H); IC50=55 nM.

후처리

  1. concentrationThe mixture is concentrated in vacuo
  2. washThe residue is washed with water and DCM

출처 및 근거

ORD 기록
ord-369611d106f543dc8e23599b32b3dc2b
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08202863B2

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