Triethylamine → HCID 86647071, 화합물

HRID 1812297노트

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HRID 1812297 반응식
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[CH3:6][O:7][C:8]1[CH:49]=[CH:48][C:11]([CH2:12][N:13]([CH2:39][C:40]2[CH:45]=[CH:44][C:43]([O:46][CH3:47])=[CH:42][CH:41]=2)[C:14]2[N:19]=[C:18]([CH3:20])[N:17]=[C:16]([C:21]3[CH:22]=[C:23]([CH:36]([OH:38])[CH3:37])[CH:24]=[N:25][C:26]=3[NH:27][C:28]3[CH:29]=[N:30][C:31]([O:34][CH3:35])=[CH:32][CH:33]=3)[N:15]=2)=[CH:10][CH:9]=1.C(N(CC)CC)C>C(Cl)Cl>[CH3:1][S:2]([O:38][CH:36]([C:23]1[CH:24]=[N:25][C:26]([NH:27][C:28]2[CH:29]=[N:30][C:31]([O:34][CH3:35])=[CH:32][CH:33]=2)=[C:21]([C:16]2[N:15]=[C:14]([N:13]([CH2:12][C:11]3[CH:10]=[CH:9][C:8]([O:7][CH3:6])=[CH:49][CH:48]=3)[CH2:39][C:40]3[CH:41]=[CH:42][C:43]([O:46][CH3:47])=[CH:44][CH:45]=3)[N:19]=[C:18]([CH3:20])[N:17]=2)[CH:22]=1)[CH3:37])(=[O:4])=[O:3]

참가 물질

5

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온도
0 °C

실험 절차

Methanesulfonyl chloride (0.164 mL, 2.119 mmol) was added to a solution of 1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-(6-methoxypyridin-3-ylamino)pyridin-3-yl)ethanol (331.1 mg, 0.558 mmol) and triethylamine (0.350 mL, 2.510 mmol) in CH2Cl2 (7.5 mL) at 0° C., and the resulting mixture was stirred at 0° C. for 30 min. The reaction mixture was then partitioned between CH2Cl2 (40 mL) and water (30 mL). The organic layer was separated, and the aqueous layer was extracted with CH2Cl2 (30 mL). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated in vacuo to provide 1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-(6-methoxypyridin-3-ylamino)pyridin-3-yl)ethyl methanesulfonate (356.1 mg, 0.530 mmol, 95% yield) as a yellow-brown solid, which was used directly in Step 3.

후처리

  1. customThe reaction mixture was then partitioned between CH2Cl2 (40 mL) and water (30 mL)
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted with CH2Cl2 (30 mL)
  4. dry with materialThe combined organic extracts were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-b7015b65eee94cd98057a03202208b0b
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08362241B2

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