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Methanesulfonic Acid → 2,3-Dihydro-2-methyl-1H-indol-1-amine monomethanesulphonate

HRID 1284966
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HRID 1284966 반응식
[NH2:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH:3]1[CH3:11].[CH3:12][S:13]([OH:16])(=[O:15])=[O:14]>C(O)(C)C>[CH3:12][S:13]([OH:16])(=[O:15])=[O:14].[NH2:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH:3]1[CH3:11]
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참가 물질

4

반응물 2

HCID 6395Methanesulfonic AcidHCID 1693151-Amino-2-methylindoline

생성물 1

HCID 441494172,3-Dihydro-2-methyl-1H-indol-1-amine monomethanesulphonate

시약·촉매·용매 1

HCID 3776Isopropanol용매

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온도
0 °C

실험 절차

10 g of crude 1-amino-2-methylindoline (made as described in Example 1) was dissolved in 40 ml of isopropanol. 6.75 g of methanesulfonic acid was added and the solution was cooled to about 0° C. to obtain crystals of 1-amino-2-methylindoline methanesulfonate which was isolated by filtration. The crystals were then washed by slurrying with fresh isopropanol and dried at 20° C. Melting range of product compound was 170°-2° C.

출처 및 근거

ORD 기록
ord-99cf2248145947fa9491aaba94b819f8
출처 데이터셋
uspto-grants-1986_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04564677

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