Aluminium lithium hydride → [2-(4-Isopropyl-4H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulen-8-yl]-methanol

HRID 2385605노트

반응식

HRID 2385605 반응식
C[O:2][C:3]([C:5]1[CH:26]=[CH:25][C:8]2[C:9]3[N:10]=[C:11]([C:17]4[N:21]([CH:22]([CH3:24])[CH3:23])[CH:20]=[N:19][N:18]=4)[S:12][C:13]=3[CH2:14][CH2:15][O:16][C:7]=2[CH:6]=1)=O.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH:22]([N:21]1[CH:20]=[N:19][N:18]=[C:17]1[C:11]1[S:12][C:13]2[CH2:14][CH2:15][O:16][C:7]3[CH:6]=[C:5]([CH2:3][OH:2])[CH:26]=[CH:25][C:8]=3[C:9]=2[N:10]=1)([CH3:24])[CH3:23]

참가 물질

4

실험 절차

To a solution of 2-(4-isopropyl-4H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-8-carboxylic acid methyl ester (620 mg, 1.67 mmol) in THF (12 mL) at 0° C. was added LiAlH4 (152 mg, 4.02 mmol). The reaction mixture was stirred for 4 hours at RT before being quenched with H2O (0.15 mL), 15% NaOH(aq) (0.15 mL) and H2O (0.45 mL). The precipitate was removed by filtration, washing with methanol/DCM, and then the filtrate was concentrated in vacuo to yield the title compound as an orange solid (563 mg, 98%). LCMS: RT=3.71 min, [M+H]+=343

후처리

  1. custombefore being quenched with H2O (0.15 mL), 15% NaOH(aq) (0.15 mL) and H2O (0.45 mL)
  2. customThe precipitate was removed by filtration
  3. washwashing with methanol/DCM
  4. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-1ce2ecf65a0f494793de82453c819f75
출처 데이터셋
uspto-grants-2012_09
특허 번호
US08263633B2

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