4-Methyl-3-nitrobenzenesulfonyl chloride → 3-(4-Methyl-3-nitrobenzenesulfonyl)-1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylic acid ethyl ester

HRID 736113노트

반응식

HRID 736113 반응식
[CH2:1]([O:3][C:4]([C:6]1[C:12]2[NH:13][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[C:11]=2[CH2:10][CH2:9][NH:8][CH:7]=1)=[O:5])[CH3:2].[CH3:20][C:21]1[CH:26]=[CH:25][C:24]([S:27](Cl)(=[O:29])=[O:28])=[CH:23][C:22]=1[N+:31]([O-:33])=[O:32]>>[CH2:1]([O:3][C:4]([C:6]1[C:12]2[NH:13][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[C:11]=2[CH2:10][CH2:9][N:8]([S:27]([C:24]2[CH:25]=[CH:26][C:21]([CH3:20])=[C:22]([N+:31]([O-:33])=[O:32])[CH:23]=2)(=[O:28])=[O:29])[CH:7]=1)=[O:5])[CH3:2]

참가 물질

3

반응물 2

HCID 5606384-Methyl-3-nitrobenzenesulfonyl chlorideHCID 57467979Ethyl 1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylate

생성물 1

HCID 575591573-(4-Methyl-3-nitrobenzenesulfonyl)-1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylic acid ethyl ester

실험 절차

The title compound was prepared in a manner similar to that described in Example 70 by using ethyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate and 4-methyl-3-nitrobenzenesulfonyl chloride (˜3.4mg); MS (ES): 456 (MH+).

출처 및 근거

ORD 기록
ord-be6f64ac271a47f6bacf8170ac85105b
출처 데이터셋
uspto-grants-2009_09
특허 번호
US07595311B2

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