2-Butyn-1-ol → HCID 58792114, 화합물

HRID 2222134노트

반응식

HRID 2222134 반응식
CS([C:5]1[N:9]=[C:8]([N:10]2[CH2:15][CH2:14][S:13][CH2:12][CH2:11]2)[S:7][N:6]=1)(=O)=O.[CH2:16]([OH:20])[C:17]#[C:18][CH3:19].[H-].[Na+]>O1CCCC1>[CH2:16]([O:20][C:5]1[N:9]=[C:8]([N:10]2[CH2:11][CH2:12][S:13][CH2:14][CH2:15]2)[S:7][N:6]=1)[C:17]#[C:18][CH3:19]

참가 물질

5

반응물 3

HCID 129912-Butyn-1-olHCID 24758Sodium hydrideHCID 69219894HCID 69219894, 화합물

생성물 1

HCID 58792114HCID 58792114, 화합물수율 64.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

In 3 ml of tetrahydrofuran were dissolved 398 mg of 3-methylsulfonyl-5-(thiomorpholino)-1,2,4-thiadiazole and 180 mg of 2-butyn-1-ol, and 102 mg of sodium hydride (oil suspension; content: 60 weight %) was added at room temperature. The mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated. The residue was subjected to recrystallization from a mixed solvent of hexane-ethyl acetate to obtain 246 mg of 3-(2-butynyloxy)-5-thiomorpholino-1,2,4-thiadiazole (hereinafter, referred to as the present compound (23)).

후처리

  1. additionwas added at room temperature
  2. concentrationThe reaction mixture was concentrated
  3. customThe residue was subjected to recrystallization from a mixed solvent of hexane-ethyl acetate

출처 및 근거

ORD 기록
ord-0d0daf32e39e4ba4b4afec08db50e435
출처 데이터셋
uspto-grants-2008_05
특허 번호
US07371746B2

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