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Tetrahydrofuran → ethyl 1-(2-aminoethyl)-1H-indazole-5-carboxylate

HRID 2252468
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HRID 2252468 반응식
O=C1C2C(=CC=CC=2)C(=O)[N:3]1[CH2:12][CH2:13][N:14]1[C:22]2[C:17](=[CH:18][C:19]([C:23]([O:25][CH2:26][CH3:27])=[O:24])=[CH:20][CH:21]=2)[CH:16]=[N:15]1.NN.C1COCC1>C(O)C.C1COCC1>[NH2:3][CH2:12][CH2:13][N:14]1[C:22]2[C:17](=[CH:18][C:19]([C:23]([O:25][CH2:26][CH3:27])=[O:24])=[CH:20][CH:21]=2)[CH:16]=[N:15]1
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참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 9321HydrazineHCID 10832532Ethyl 1-[2-(1,3-dioxoisoindolin-2-yl)ethyl]-1H-indazole-5-carboxylate

생성물 1

HCID 10585718ethyl 1-(2-aminoethyl)-1H-indazole-5-carboxylate

시약·촉매·용매 1

HCID 21873804Tetrahydrofuran ethanol용매

실험 절차

Ethyl 1-[2-(1,3-dioxoisoindolin-2-yl)ethyl]-1H-indazole-5-carboxylate (step A, 980 mg, 2.7 mmol) was dissolved in ethanol/THF (1:1, 35 mL) under nitrogen. Hydrazine (365 uL) was added and the reaction stirred 17 hours. THF (75 mL) was added and the resulting solids were filtered off. The filtrate was concentrated to an orange solid, which was purified by flash chromatography (dichoromethane/5% methanol/0.5% triethylamine). The product fractions were combined and concentrated to an orange solid (404 mg, 66%). LRMS (ES): 234.1 ([M+H]+, 100%).

후처리

  1. filtrationthe resulting solids were filtered off
  2. concentrationThe filtrate was concentrated to an orange solid, which
  3. customwas purified by flash chromatography (dichoromethane/5% methanol/0.5% triethylamine)
  4. concentrationconcentrated to an orange solid (404 mg, 66%)

출처 및 근거

ORD 기록
ord-f0d6551c9f1d4c0382ffe7a430945bdc
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07321045B2

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