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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 14467914, 화합물 → HCID 58659580, 화합물

HRID 854115
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HRID 854115 반응식
N1C=CC=[CH:3][C:2]=1[CH2:7][S@@:8]([C:10]([CH3:13])([CH3:12])[CH3:11])=[O:9].N1C=CC=C[C:15]=1C[Li]>C1COCC1>[CH2:7]([S@:8]([C:10]([CH3:11])([CH3:12])[CH3:13])=[O:9])[CH:2]([CH3:3])[CH3:15]
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참가 물질

4

반응물 2

HCID 14467914HCID 14467914, 화합물HCID 178506852HCID 178506852, 화합물

생성물 1

HCID 58659580HCID 58659580, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Preparation of (S)-picolinyl t-butylsulfoxide from (S)-tert-Butyl (1R, 2S)-aminoindanol 4-toluene sulfonamide sulfinate: To a picolinyl lithium solution (2 mL, 0.6 M) in THF at −78° C. was added (S)-t-butyl-(1R, 2S)-aminoindanol tosylate sulfinate (130 mg, 0.30 mmol). The mixture was warmed to room temperature and stirred until the starting material was consumed as monitored by TLC. The reaction was quenched by aq. NaHCO3 (20 mL) and diluted with ethyl acetate (20 mL), and the organic phase was washed with water (20 mL) and brine (20 mL). The organic layer was concentrated in vacuo and the residue was purified by chromatography eluted with ethyl acetate to yield 32 mg of the desired product.

후처리

  1. customwas consumed
  2. customThe reaction was quenched by aq. NaHCO3 (20 mL)
  3. additiondiluted with ethyl acetate (20 mL)
  4. washthe organic phase was washed with water (20 mL) and brine (20 mL)
  5. concentrationThe organic layer was concentrated in vacuo
  6. customthe residue was purified by chromatography
  7. washeluted with ethyl acetate

출처 및 근거

ORD 기록
ord-5ccc389c81d04c8caf6bfead3b78ebf8
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07256297B2

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