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Diisopropylethylamine → 7-Bromo[1,2,4]triazolo[1,5-a]pyridin-2-amine

HRID 1802201
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HRID 1802201 반응식
Cl.NO.C([N:6](C(C)C)C(C)C)C.C(OC([NH:18][C:19]([NH:21][C:22]1[CH:27]=[C:26]([Br:28])[CH:25]=[CH:24][N:23]=1)=S)=O)C>C(O)C>[Br:28][C:26]1[CH:25]=[CH:24][N:23]2[N:6]=[C:19]([NH2:18])[N:21]=[C:22]2[CH:27]=1
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참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 443297Hydroxyamine hydrochlorideHCID 57643101HCID 57643101, 화합물

생성물 1

HCID 545940257-Bromo[1,2,4]triazolo[1,5-a]pyridin-2-amine수율 87.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of hydroxylamine hydrochloride (20.0 g, 288 mmol) and N-ethyldiisopropylamine (30.1 ml, 173 mmol) in ethanol (367 ml) is stirred for a few minutes at room temperature and the mixture is added to 1-ethoxycarbonyl-3-(4-bromo-pyridin-2-yl)-thiourea (17.5 g, 57.5 mmol). The resulting mixture is refluxed for 1 day. The solvent is evaporated and 100 ml water is added to the residue. The suspension is stirred for 10 minutes, the solid is collected by filtration, washed with water and dried affording 7-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine (10.71 g, 87.4%) as a light yellow solid. Mp.: 190-2° C. MS: m/z=213.0, 215.0 (M+H+).

후처리

  1. temperatureThe resulting mixture is refluxed for 1 day
  2. customThe solvent is evaporated
  3. addition100 ml water is added to the residue
  4. stirringThe suspension is stirred for 10 minutes
  5. filtrationthe solid is collected by filtration
  6. washwashed with water
  7. customdried

출처 및 근거

ORD 기록
ord-afa48e4c5ab44df6a07a1212b8426b53
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08349824B2

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