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2-Propanaminium, N,N,N-tris(1,1-dimethylethyl)-2-methyl-, fluoride → 3-((trans-4-hydroxy-2-(S)-pyrrolidinyl)methoxy)pyridine

HRID 617343
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HRID 617343 반응식
C([N:11]1[CH2:15][C@H:14]([O:16][Si](C(C)(C)C)(C)C)[CH2:13][C@H:12]1[CH2:24][O:25][C:26]1[CH:27]=[N:28][CH:29]=[CH:30][CH:31]=1)(OCC1C=CC=CC=1)=O.[F-].C([N+](C(C)(C)C)(C(C)(C)C)C(C)(C)C)(C)(C)C>C1COCC1>[OH:16][C@H:14]1[CH2:15][NH:11][C@H:12]([CH2:24][O:25][C:26]2[CH:27]=[N:28][CH:29]=[CH:30][CH:31]=2)[CH2:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 108690552-Propanaminium, N,N,N-tris(1,1-dimethylethyl)-2-methyl-, fluorideHCID 18391718trans-3-((1-CBZ4-(t-butyldimethylsilyloxy)-2-(S)-pyrrolidinyl)methoxy)pyridine

생성물 1

HCID 542026473-((trans-4-hydroxy-2-(S)-pyrrolidinyl)methoxy)pyridine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A 1.35 g sample of the compound from step 72d above was dissolved in 9 mL of THF and 9.3 mL of tetra-(t-butyl)ammonium fluoride was added. The reaction mixture was stirred at room temperature for 16 hours, and the volatiles were removed under vacuum. The residue was purified on silica gel, eluting with 3:1 ethyl acetate:hexane, to give the title compound.

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후처리

  1. customthe volatiles were removed under vacuum
  2. customThe residue was purified on silica gel
  3. washeluting with 3:1 ethyl acetate

출처 및 근거

ORD 기록
ord-7712e5a6f0ea4df39c74ad34728a088d
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05948793

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