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Ammonium Hydroxide → 2-(4-Isopropylpiperazin-1-yl)benzothiazole

HRID 1619266
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반응식

HRID 1619266 반응식
[CH:1]([N:4]1[CH2:9][CH2:8][N:7]([C:10]2[S:11][C:12]3[CH:18]=[CH:17][C:16](C#N)=[CH:15][C:13]=3[N:14]=2)[CH2:6][CH2:5]1)([CH3:3])[CH3:2].[NH4+].[OH-]>CO.C1COCC1.[Ni]>[CH:1]([N:4]1[CH2:5][CH2:6][N:7]([C:10]2[S:11][C:12]3[CH:18]=[CH:17][CH:16]=[CH:15][C:13]=3[N:14]=2)[CH2:8][CH2:9]1)([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14923Ammonium HydroxideHCID 237288942-(4-Isopropylpiperazin-1-yl)benzothiazole-5-carbonitrile

생성물 1

HCID 106114582-(4-Isopropylpiperazin-1-yl)benzothiazole수율 110.8%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 21899815MeOH tetrahydrofuran용매

실험 절차

To a solution of 2-(4-isopropylpiperazin-1-yl)benzothiazole-5-carbonitrile (500 mg, 1.75 mmol) in MeOH-THF (66 mL, 3:5) was added NH4OH (7 mL) and Raney Ni (100 mg). The mixture was stirred for 12 h at rt under a H2 atmosphere. The mixture was filtered and the filtrate was concentrated to give 5-aminomethyl-[2-(4-isopropylpiperazin-1-yl)benzothiazole 507 mg (100%), which was used in the next step without further purification.

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후처리

  1. filtrationThe mixture was filtered
  2. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-74aaf0a6dd044115a7254674c7c5e1e8
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772285B2

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