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Methanol → HCID 59828901, 화합물

HRID 1191061
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HRID 1191061 반응식
[CH3:1][N:2]([CH3:14])[C:3]([S:5][C:6]1[CH:13]=[CH:12][C:9]([C:10]#[N:11])=[CH:8][CH:7]=1)=[O:4].B.CSC.CO.[H][H]>C1COCC1>[CH3:1][N:2]([CH3:14])[C:3]([S:5][C:6]1[CH:13]=[CH:12][C:9]([CH2:10][NH2:11])=[CH:8][CH:7]=1)=[O:4]
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참가 물질

6

반응물 4

HCID 887MethanolHCID 5516014-dimethylcarbamoylthio-benzonitrileHCID 12423031(Dimethyl sulfide)trihydroboronHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 59828901HCID 59828901, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Dissolve 4-dimethylcarbamoylthio-benzonitrile (3.07 g, 14.9 mmol) in anhydrous THF (30 mL). Add borane-dimethylsulfide complex (4.24 mL, 44.7 mmol, 1M solution in diethyl ether) and stir the mixture at room temperature for 3 h. Add methanol dropwise until hydrogen evolution ceases. Concentrate the mixture in vacuo and purify the crude mixture by SCX chromatography eluting with methanol and 2M ammonia in methanol to obtain the title compound as a slightly impure oil (2.9 g). Dissolve the oil (2.9 g) in DCM and add 2M hydrogen chloride in ether. Stir the mixture for 1 h and concentrate in vacuo to obtain a solid. Suspend the solid in DCM and add diethyl ether to precipitate the salt. Filter and dry the solid in vacuo to obtain the hydrochloride salt of the title compound as a white solid (2.33 g, 64%). Elute the compound through a SCX column to obtain the desired intermediate as an oil. MS (ES+) m/z: 211 (M+H)+.

후처리

  1. concentrationConcentrate the mixture in vacuo
  2. custompurify the crude mixture by SCX chromatography
  3. washeluting with methanol and 2M ammonia in methanol

출처 및 근거

ORD 기록
ord-ee40b95e32644154a0e130c1790950db
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680091B2

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