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1,1'-Carbonyldiimidazole → HCID 22626834, 화합물

HRID 277907
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HRID 277907 반응식
[Cl:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Cl:12])[C:7]=1[CH2:8][C:9]([OH:11])=O.C(N1C=CN=C1)(N1C=CN=C1)=O.[CH3:25][O:26][C:27]1[CH:28]=[C:29]([CH:33]([CH2:36][CH:37]([CH3:39])[CH3:38])[CH2:34][NH2:35])[CH:30]=[CH:31][CH:32]=1>C1COCC1>[Cl:12][C:6]1[CH:5]=[N:4][CH:3]=[C:2]([Cl:1])[C:7]=1[CH2:8][C:9]([NH:35][CH2:34][CH:33]([C:29]1[CH:30]=[CH:31][CH:32]=[C:27]([O:26][CH3:25])[CH:28]=1)[CH2:36][CH:37]([CH3:39])[CH3:38])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 682631,1'-CarbonyldiimidazoleHCID 22626827HCID 22626827, 화합물HCID 226268442-(3-Methoxy-phenyl)-4-methyl-pentylamine

생성물 1

HCID 22626834HCID 22626834, 화합물수율 97.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

By working in a way similar to that described in example 4 but using (3,5-dichloropyridin-4-yl)-acetic acid (2.06 g, 10 mmoles), carbonyldiimidazole (1.78 g, 11 mmoles), THF (30 ml) and 2-(3-methoxy-phenyl)-4-methyl-pentylamine (2.07 g, 10 mmoles), obtained as described in example 21, 3.85 g of the title compound were obtained (yield: 97.6%), m.p.: 98-99° C.

후처리

  1. customobtained

출처 및 근거

ORD 기록
ord-8f0852674e6949dba88b72a63e558070
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06358973B1

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