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HCID 67812897, 화합물 → [6-(2-Cyclopentylsulfanyl-pyridin-3-ylmethoxy)-7-methyl-benzofuran-3-yl]-acetic acid

HRID 62989
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인쇄 미리보기

반응식

HRID 62989 반응식
Cl[CH2:2][C:3]1[C:4]([S:9][CH:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)=[N:5][CH:6]=[CH:7][CH:8]=1.C[O:16][C:17](=[O:30])[CH2:18][C:19]1[C:23]2[CH:24]=[CH:25][C:26]([OH:29])=[C:27]([CH3:28])[C:22]=2[O:21][CH:20]=1>>[CH:10]1([S:9][C:4]2[C:3]([CH2:2][O:29][C:26]3[CH:25]=[CH:24][C:23]4[C:19]([CH2:18][C:17]([OH:30])=[O:16])=[CH:20][O:21][C:22]=4[C:27]=3[CH3:28])=[CH:8][CH:7]=[CH:6][N:5]=2)[CH2:14][CH2:13][CH2:12][CH2:11]1
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참가 물질

3

반응물 2

HCID 67812897HCID 67812897, 화합물HCID 901182833-Chloromethyl-2-cyclopentylsulfanyl-pyridine

생성물 1

HCID 74221672[6-(2-Cyclopentylsulfanyl-pyridin-3-ylmethoxy)-7-methyl-benzofuran-3-yl]-acetic acid수율 83.9%

실험 절차

3-Chloromethyl-2-cyclopentylsulfanyl-pyridine (21 mg, 0.09 mmol) obtained in Step C of Preparation Example 8 and (6-hydroxy-7-methyl-benzofuran-3-yl)-acetic acid methyl ester (21 mg, 0.09 mmol) obtained in Preparation Example 54 were used to react sequentially in the same manner as in Steps A and B of Example 1 to obtain the title compound (30 mg, 83%).

후처리

  1. customobtained in Preparation Example 54
  2. customto react sequentially in the same manner as in Steps A and B of Example 1

출처 및 근거

ORD 기록
ord-4b9a8b2ef709491abe4fe00f58bc3137
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09447044B2

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