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1,1'-Carbonyldiimidazole → N-[3-(4-Iodo-2-methyl-phenylamino)-pyridine-4-carbonyl]methanesulfonamide

HRID 39603
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HRID 39603 반응식
[I:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[CH:17]=[N:16][CH:15]=[CH:14][C:10]=2[C:11](O)=[O:12])=[C:4]([CH3:18])[CH:3]=1.C(N1C=CN=C1)(N1C=CN=C1)=O.[CH3:31][S:32]([NH2:35])(=[O:34])=[O:33].C1CCN2C(=NCCC2)CC1>C1COCC1>[I:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[CH:17]=[N:16][CH:15]=[CH:14][C:10]=2[C:11]([NH:35][S:32]([CH3:31])(=[O:34])=[O:33])=[O:12])=[C:4]([CH3:18])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 682631,1'-CarbonyldiimidazoleHCID 72879MethanesulfonamideHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 576496173-[(2-Methyl-4-iodophenyl)amino]isonicotinic acid

생성물 1

HCID 57649648N-[3-(4-Iodo-2-methyl-phenylamino)-pyridine-4-carbonyl]methanesulfonamide수율 33%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

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온도
40 °C

실험 절차

3-[(4-Iodo-2-methylphenyl)amino]isonicotinic acid (example 3) (50 mg, 0.141 mmol) was dissolved in 4 ml dry THF followed by the addition of 1,1′-carbonyldiimidazole (CDI) (0.311 mmol, 50 mg), methanesulfonamide (0.169 mmol, 16.1 mg) and DBU (0.169 mmol, 26 mg). The mixture was stirred for 16 h at 40° C. and the volatiles were removed in vacuo. The crude material was purified by preparative HPLC to give 20.3 mg (47 μmol; 33% yield) of pure desired product. LC-MS (method III): rt=2.74 min; m/z [M+H]+ 432.

후처리

  1. customthe volatiles were removed in vacuo
  2. customThe crude material was purified by preparative HPLC

출처 및 근거

ORD 기록
ord-156640adc5b1445284fc456d8a7d1b9d
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524911B2

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