(+-)-1-Aminoindan → HCID 18627820, 화합물

HRID 1418086노트

반응식

HRID 1418086 반응식
[NH2:1][CH:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3]1.[CH2:11]([N:14]([CH2:27][CH2:28][CH3:29])[S:15]([C:18]1[CH:26]=[CH:25][C:21]([C:22](Cl)=[O:23])=[CH:20][CH:19]=1)(=[O:17])=[O:16])[CH2:12][CH3:13]>>[CH2:27]([N:14]([CH2:11][CH2:12][CH3:13])[S:15]([C:18]1[CH:26]=[CH:25][C:21]([C:22]([NH:1][CH:2]2[C:10]3[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=3)[CH2:4][CH2:3]2)=[O:23])=[CH:20][CH:19]=1)(=[O:17])=[O:16])[CH2:28][CH3:29]

참가 물질

3

반응물 2

HCID 123445(+-)-1-AminoindanHCID 27355284-(Dipropylsulfamoyl)benzoyl chloride

생성물 1

HCID 18627820HCID 18627820, 화합물수율 63%

실험 절차

The title compound was prepared in 63% yield from (rac)-1-aminoindan (10.0 g, 75.2 mmole) and 4-(di-n-propylsulfamoyl) benzoyl chloride (16.3 g, 53.6 mmole, prepared from probenecid and SOCl2) via a procedure analogous to that described in Ex. 46, followed by crystallization from hexane:EtOAc, mp: 124°-5° C.

후처리

  1. custom46, followed by crystallization from hexane

출처 및 근거

ORD 기록
ord-37205c879f7d488baa7134d7dd3f956d
출처 데이터셋
uspto-grants-1999_03
특허 번호
US05880159

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