8-Allyl-1-ethyl-7-fluoro-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid methyl ester → 8-Allyl-1-ethyl-7-fluoro-4-oxo-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid methyl ester

HRID 1955721노트

반응식

HRID 1955721 반응식
[CH3:1][O:2][C:3](=[O:24])[CH2:4][C:5]1([CH2:22][CH3:23])[C:10]2[NH:11][C:12]3[C:17]([C:9]=2[CH2:8][CH2:7][O:6]1)=[CH:16][CH:15]=[C:14]([F:18])[C:13]=3[CH2:19][CH:20]=[CH2:21].CC1(C)N([O])C(C)(C)CCC1.F[B-](F)(F)F.CC#N.[OH2:44]>>[CH3:1][O:2][C:3](=[O:24])[CH2:4][C:5]1([CH2:22][CH3:23])[C:10]2[NH:11][C:12]3[C:17]([C:9]=2[C:8](=[O:44])[CH2:7][O:6]1)=[CH:16][CH:15]=[C:14]([F:18])[C:13]=3[CH2:19][CH:20]=[CH2:21]

참가 물질

4

반응물 3

HCID 147700108-Allyl-1-ethyl-7-fluoro-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid methyl esterHCID 18373917Acetonitrile--water (1/1)2회HCID 178424956HCID 178424956, 화합물

생성물 1

HCID 676190068-Allyl-1-ethyl-7-fluoro-4-oxo-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid methyl ester

실험 절차

A solution of the ester (0.21 g, 0.63 mmol, prepared as described in Step A), in 10 ml of CH3CN--H2O (9:1, v/v) was added dropwise to a stirred solution of TEMPO-BF4 in 10 ml CH3CN--H2O (9:1, v/v). Stirring was continued for 2 h and the reaction mixture was concentrated in vacuo. The residue was partitioned between Et2O and H2O. The organic phase was washed with brine and dried (Na2 SO4). Removal of solvent provides a yellow oil which was purified by flash chromatography (silica gel, hexane- EtOAc 2:1) to give 0.18 g of product as an off white solid.

후처리

  1. concentrationthe reaction mixture was concentrated in vacuo
  2. customThe residue was partitioned between Et2O and H2O
  3. washThe organic phase was washed with brine
  4. customdried (Na2 SO4)
  5. customRemoval of solvent
  6. customprovides a yellow oil which
  7. customwas purified by flash chromatography (silica gel, hexane- EtOAc 2:1)

출처 및 근거

ORD 기록
ord-a8e1817b9af242fdb2a67b231e22c8a4
출처 데이터셋
uspto-grants-1998_07
특허 번호
US05776967

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