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Methanesulfonic Acid → HCID 25195527, 화합물

HRID 1436944
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인쇄 미리보기

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HRID 1436944 반응식
[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:19])[CH3:18])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4].[CH3:23][S:24]([OH:27])(=[O:26])=[O:25]>O>[S:24]([OH:27])(=[O:26])(=[O:25])[CH3:23].[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:18])[CH3:19])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6395Methanesulfonic AcidHCID 11716529HCID 11716529, 화합물

생성물 1

HCID 25195527HCID 25195527, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a suspension of compound (3) (4.44 g, 14.3 mmol) in H2O (100 mL) was added methanesulfonic acid (0.93 mL, 14.3 mmol). The resulting mixture was stirred at room temperature until the solid had completely dissolved. The solution was then frozen and lyophilized to afford the desired product as a light pinkish solid.

후처리

  1. dissolutionhad completely dissolved
  2. temperature
The solution was then frozen

출처 및 근거

ORD 기록
ord-db21fdc496b54fceaadb8634386f1e02
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07619110B2

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