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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Cysteamine Hydrochloride → HCID 87903836, 화합물

HRID 1824683
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HRID 1824683 반응식
C(=O)(O)[O-].[Na+].Cl.[NH2:7][CH2:8][CH2:9][SH:10].[C:11]([O:15][C:16](=[O:25])[NH:17][C@H:18]([C:22](F)=[O:23])[CH:19]([CH3:21])[CH3:20])([CH3:14])([CH3:13])[CH3:12]>O.C(Cl)Cl>[C:11]([O:15][C:16](=[O:25])[NH:17][C@H:18]([C:22](=[O:23])[NH:7][CH2:8][CH2:9][SH:10])[CH:19]([CH3:20])[CH3:21])([CH3:12])([CH3:14])[CH3:13]
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참가 물질

6

반응물 3

HCID 9082Cysteamine HydrochlorideHCID 516892Sodium BicarbonateHCID 10751345t-Butoxycarbonylvaline fluoride

생성물 1

HCID 87903836HCID 87903836, 화합물

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매

실험 절차

To a 50 mL round-bottom flask charged with a solution of sodium bicarbonate (158.1 mg, 1.88 mmol) in 9.2 mL water was added 2-aminoethanethiol hydrochloride (114.7 mg, 1.01 mmol). To this stirring solution was added dropwise over 60 seconds a solution of 25g (201.3 mg, 0.92 mmol) in 9.2 mL CH2Cl2. The reaction was vigorously stirred for 25 minutes at room temperature, then extracted twice with fresh CH2Cl2. The combined CH2Cl2 extracts were washed once with 5% aqueous HCl, once with 10% aqueous sodium bicarbonate, then once with water. The organic fraction was dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo, to afford 222.0 mg (80% from 24g) of clean 26g as a colorless oil. FTIR (neat) 3300, 1681, 1652 cm−1.

후처리

  1. extractionextracted twice with fresh CH2Cl2
  2. washThe combined CH2Cl2 extracts were washed once with 5% aqueous HCl, once with 10% aqueous sodium bicarbonate
  3. dry with materialThe organic fraction was dried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-8e88a74688c54a8fa47d402268293af5
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07045360B2

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