Ammonium Chloride → HCID 21897393, 화합물

HRID 719872노트

반응식

HRID 719872 반응식
[N+:1]([C:4]1[N:5]=[CH:6][C:7]([NH:10][S:11]([CH3:14])(=[O:13])=[O:12])=[N:8][CH:9]=1)([O-])=O.[Cl-].[NH4+]>CO.O.[Zn]>[NH2:1][C:4]1[N:5]=[CH:6][C:7]([NH:10][S:11]([CH3:14])(=[O:13])=[O:12])=[N:8][CH:9]=1

참가 물질

6

반응물 2

HCID 25517Ammonium ChlorideHCID 21897390N-(5-nitro-pyrazin-2-yl)-methanesulfonamide

생성물 1

HCID 21897393HCID 21897393, 화합물수율 109.2%

시약·촉매·용매 3

HCID 23994Zinc촉매HCID 887Methanol용매HCID 962Water용매

반응 조건

온도
25 °C

실험 절차

A solution of N-(5-nitro-pyrazin-2-yl)-methanesulfonamide (583.9 mg, 2.67 mmol) in methanol (26.8 mL) was treated with a solution of ammonium chloride (300.6 mg, 5.62 mmol) in water (2 mL). This solution was stirred at 25° C. for 5 min. At this time, the reaction was treated with zinc dust (1.71 g, 26.2 mmol). The resulting mixture was heated under reflux for 2 h. At this time, the reaction was cooled to 25° C. and was filtered through a pad of silica gel (9/1 methylene chloride/methanol wash). The filtrate was concentrated in vacuo to afford N-(5-amino-pyrazin-2-yl)-methanesulfonamide (548.8 mg, 100%) as a dark-brown gum: EI-HRMS m/e calcd for C5H8N4O2S (M+H)+ 189.0441, found 189.0442.

후처리

  1. temperatureThe resulting mixture was heated
  2. temperatureunder reflux for 2 h
  3. temperatureAt this time, the reaction was cooled to 25° C.
  4. filtrationwas filtered through a pad of silica gel (9/1 methylene chloride/methanol wash)
  5. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-a901d0deaa1c4cb0a929fefb77e56629
출처 데이터셋
uspto-grants-2006_11
특허 번호
US07132425B2

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