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Water → N,N-diethyl-5-(1-methyl-1H-indol-2-yl)pyridine-3-sulfonamide

HRID 593691
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HRID 593691 반응식
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]1B(O)O.Br[C:15]1[CH:16]=[C:17]([S:21]([N:24]([CH2:27][CH3:28])[CH2:25][CH3:26])(=[O:23])=[O:22])[CH:18]=[N:19][CH:20]=1.C([O-])([O-])=O.[K+].[K+].O>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CN(C=O)C.O1CCOCC1>[CH2:27]([N:24]([CH2:25][CH3:26])[S:21]([C:17]1[CH:18]=[N:19][CH:20]=[C:15]([C:3]2[N:2]([CH3:1])[C:10]3[C:5]([CH:4]=2)=[CH:6][CH:7]=[CH:8][CH:9]=3)[CH:16]=1)(=[O:22])=[O:23])[CH3:28]
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참가 물질

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반응물 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 198548155-Bromo-N,N-diethylpyridine-3-sulfonamideHCID 22733820(1-Methyl-1H-indol-2-yl)boronic acid

생성물 1

HCID 58215618N,N-diethyl-5-(1-methyl-1H-indol-2-yl)pyridine-3-sulfonamide

시약·촉매·용매 3

HCID 178418397
HCID 178418397, 화합물
촉매
HCID 6228Dimethylformamide용매
HCID 312751,4-Dioxane용매

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온도
90 °C

실험 절차

A flask is charged with 1-methyl-1H-indol-2-ylboronic acid (90 mg, 0.512 mmol), 5-bromo-N,N-diethylpyridine-3-sulfonamide (100 mg, 0.341 mmol) and polymer supported Pd(PPh3)4 (189 mg, 0.017 mmol), and the flask is flushed with N2 for 5 min. 1,4-Dioxane (10 mL) and 2M K2CO3 in water (0.512 mL, 1.023 mmol) are added under N2 and the mixture is stirred at 90° C. under N2 for 2 h. The mixture is then cooled to room temperature and DMF (4 mL) is added. The mixture is concentrated in vacuo and the residue is filtered and the filtrate is purified by Xterra RP18 eluting with a 1:9 to 9:1 acetonitrile-water gradient to give N,N-diethyl-5-(1-methyl-1H-indol-2-yl)pyridine-3-sulfonamide. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.10 (t, J=7.1 Hz, 6H), 3.29 (d, J=7.1 Hz, 4H), 3.80 (s, 3H), 6.85 (s, 1H), 7.08-7.14 (m, 1H), 7.26 (td, J=7.71, 1.26 Hz, 1H), 7.56 (dd, J=8.3, 0.5 Hz, 1H), 7.63 (d, J=7.8 Hz, 1H), 8.33 (t, J=2.1 Hz, 1H), 9.00 (d, J=2.0 Hz, 1H), 9.10 (d, J=2.2 Hz, 1H). HRMS: (ESI) m/z 344.1428 [(M+H)+ Calcd for C18H22N3O2S 344.1427].

후처리

  1. customthe flask is flushed with N2 for 5 min
  2. temperatureThe mixture is then cooled to room temperature
  3. concentrationThe mixture is concentrated in vacuo
  4. filtrationthe residue is filtered
  5. customthe filtrate is purified by Xterra
  6. washRP18 eluting with a 1:9 to 9:1 acetonitrile-water gradient

출처 및 근거

ORD 기록
ord-2be87e8f953e412ab77fd799bd4ab49e
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242963B2

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