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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 69242804, 화합물 → HCID 11675251, 화합물

HRID 2242187
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HRID 2242187 반응식
C(OC([N:8]1[CH2:12][C@@H:11]([CH2:13][NH:14][C:15](=[O:26])[C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([C:22]([O:24][CH3:25])=[O:23])[CH:17]=2)[CH2:10][C@H:9]1[C:27]([N:29]1[CH2:33][CH2:32][S:31][CH2:30]1)=[O:28])=O)(C)(C)C>Cl.O1CCOCC1>[CH3:25][O:24][C:22](=[O:23])[C:18]1[CH:19]=[CH:20][CH:21]=[C:16]([C:15]([NH:14][CH2:13][C@H:11]2[CH2:10][C@@H:9]([C:27]([N:29]3[CH2:33][CH2:32][S:31][CH2:30]3)=[O:28])[NH:8][CH2:12]2)=[O:26])[CH:17]=1
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참가 물질

4

반응물 1

HCID 69242804HCID 69242804, 화합물

생성물 1

HCID 11675251HCID 11675251, 화합물

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

실험 절차

A solution of Example 18A (100 mg) in 4 M HCl in dioxane (2 mL) was stirred at room temperature for 16 hours, and concentrated under reduced pressure. The residue was taken up and concentrated under reduced pressure under the following solvents, methanol (10 mL), ether (10 mL) and dichloromethane (10 mL) to provide the titled compound as a pale yellow solid. MS (ESI) m/e 378 (M+H)+; 1H NMR (500 MHz, CD3OD): δ ppm 1.80 (m, 1 H), 2.74 (m, 1 H), 2.82 (m, 1 H), 3.09 (m, 1 H), 3.16 (q, 1 H), 3.23 (dd, 1 H), 3.33 (m, 1 H), 3.56 (m, 3 H), 3.74 (m, 1 H), 3.88 (m, 1 H), 3.93 (d, 3 H), 4.52 (m, 1 H), 4.67 (m, 2 H), 7.61 (m, 1 H), 8.07 (m, 1 H), 8.19 (d, 1 H), 8.49 (m, 1 H).

후처리

  1. concentrationconcentrated under reduced pressure
  2. concentrationconcentrated under reduced pressure under the following solvents, methanol (10 mL), ether (10 mL) and dichloromethane (10 mL)

출처 및 근거

ORD 기록
ord-a5caf3ebcddd420c9b542deafb2fc107
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07671076B2

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