Water → Dimethylcarbamic acid 3-{3-((tert-butoxycarbonyl)aminosulfonyl)aminobenzyl}-6-chloro-4-fluoromethyl-2-oxo-2H-1-benzopyran-7-yl ester

HRID 599834노트

반응식

HRID 599834 반응식
C(N(CC)CC)C.[C:8]([O:12][C:13]([N-:15][S:16](N1C=CC(=[N+](C)C)C=C1)(=[O:18])=[O:17])=[O:14])([CH3:11])([CH3:10])[CH3:9].[NH2:28][C:29]1[CH:30]=[C:31]([CH:53]=[CH:54][CH:55]=1)[CH2:32][C:33]1[C:34](=[O:52])[O:35][C:36]2[CH:44]=[C:43]([O:45][C:46](=[O:50])[N:47]([CH3:49])[CH3:48])[C:42]([Cl:51])=[CH:41][C:37]=2[C:38]=1[CH2:39][F:40].O>ClCCl>[C:8]([O:12][C:13]([NH:15][S:16]([NH:28][C:29]1[CH:30]=[C:31]([CH:53]=[CH:54][CH:55]=1)[CH2:32][C:33]1[C:34](=[O:52])[O:35][C:36]2[CH:44]=[C:43]([O:45][C:46](=[O:50])[N:47]([CH3:49])[CH3:48])[C:42]([Cl:51])=[CH:41][C:37]=2[C:38]=1[CH2:39][F:40])(=[O:18])=[O:17])=[O:14])([CH3:11])([CH3:9])[CH3:10]

참가 물질

6

실험 절차

Triethylamine (34 μL, 0.25 mmol) and N-(tert-butoxycarbonyl)-N-{4-(dimethylazaniumylidene)-1,4-dihydropyridin-1-ylsulfonyl}azanide (49 mg, 0.16 mmol) were added in series to a solution of dimethylcarbamic acid 3-(3-aminobenzyl)-6-chloro-4-fluoromethyl-2-oxo-2H-1-benzopyran-7-yl ester (compound 1h-1-3F) (33 mg, 0.082 mmol) in anhydrous dichloromethane (1.0 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was then poured into water and extracted with ethyl acetate. The organic extract was washed with saturated saline and dried over magnesium sulfate. A crude solid was then obtained by vacuum concentration, and purified by preparative TLC (ethyl acetate:hexane=1:2) to yield the title compound (30 mg, 63%) as a white powder.

후처리

  1. extractionextracted with ethyl acetate
  2. extractionThe organic extract
  3. washwas washed with saturated saline
  4. dry with materialdried over magnesium sulfate
  5. customA crude solid was then obtained by vacuum concentration
  6. custompurified by preparative TLC (ethyl acetate:hexane=1:2)

출처 및 근거

ORD 기록
ord-62cf9484c72d4c61bde37eccf51d8d2c
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07897792B2

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