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Triethylamine → N-[2-(2-cyclopentyloxy-3-methoxy-phenyl)-ethyl]-2-pyridin-4-yl-acetamide

HRID 378980
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반응식

HRID 378980 반응식
Cl.[CH:2]1([O:7][C:8]2[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[CH:10][C:9]=2[CH2:16][CH2:17][NH2:18])[CH2:6][CH2:5][CH2:4][CH2:3]1.C([N:21]([CH2:24][CH3:25])[CH2:22][CH3:23])C.Cl.[C:27](O)(=[O:34])[C:28]1C=CN=C[CH:29]=1>[Cl-]>[CH:2]1([O:7][C:8]2[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[CH:10][C:9]=2[CH2:16][CH2:17][NH:18][C:27](=[O:34])[CH2:28][C:29]2[CH:23]=[CH:22][N:21]=[CH:24][CH:25]=2)[CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 216972672-(2-Cyclopentyloxy-3-methoxy-phenyl)-ethylamine HydrochlorideHCID 57455229HCID 57455229, 화합물

생성물 1

HCID 21697280N-[2-(2-cyclopentyloxy-3-methoxy-phenyl)-ethyl]-2-pyridin-4-yl-acetamide수율 108.9%

시약·촉매·용매 1

HCID 312Chloride용매

실험 절차

Operating analogously to example 46 using 2-(2-cyclopentyloxy-3-methoxy-phenyl)-ethylamine hydrochloride (1 g, 3.68 mmoles), obtained as described in example 3, in methliene chloride (20 ml), triethylamine (1.69 ml, 1.23 g, 12.14 mmoles) and isonicotinic acid hydrochloride (0.72 g, 4.05 mmoles), 1.42 g of the title product were obtained (yield: 99.9%).

후처리

  1. customobtained

출처 및 근거

ORD 기록
ord-41f80ffdfcb5458bb01cf4be5535787a
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06297257B1

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