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Ammonium Hydroxide → 3-Chloro-5-methoxybenzo[b]thiophene-2-carboxamide

HRID 2226850
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반응식

HRID 2226850 반응식
[Cl:1][C:2]1[C:3]2[CH:13]=[C:12]([O:14][CH3:15])[CH:11]=[CH:10][C:4]=2[S:5][C:6]=1[C:7](Cl)=[O:8].[NH4+:16].[OH-]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[C:3]2[CH:13]=[C:12]([O:14][CH3:15])[CH:11]=[CH:10][C:4]=2[S:5][C:6]=1[C:7]([NH2:16])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 101991093-Chloro-5-methoxybenzo[b]thiophene-2-carbonyl chloride

생성물 1

HCID 106815953-Chloro-5-methoxybenzo[b]thiophene-2-carboxamide

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a suspension of 3-chloro-5-methoxybenzo[b]thiophene-2-carbonyl chloride (1.52 g, 5.82 mmol) [Connor D. T., et al., J. Med. Chem. 35, 935 (1992)] in 80 mL of toluene at 50° C. is added dropwise 10 mL of aqueous NH4OH. The resulting precipitate is collected by filtration and recrystallized from methanol to provide 3-chloro-5-methoxybenzo[b]thiophene2-carboxamide; mp=220°-222° C.

후처리

  1. filtrationThe resulting precipitate is collected by filtration
  2. customrecrystallized from methanol

출처 및 근거

ORD 기록
ord-abee970752414950a23fc988f3a26d63
출처 데이터셋
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05350748

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