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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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diethyl 3,4-dihydro-7-[3-(4-chlorophenoxy)propoxy]-4-oxo-8-propyl-2H-1-benzopyran-2,2-dipropanoate → 7-[3-[(4-chloro-1-naphthalenyl)oxy]propoxy]-3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-2,2-dipropanoic acid

HRID 2371621
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인쇄 미리보기

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HRID 2371621 반응식
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:13][CH2:14][CH2:15][O:16][C:17]2[CH:41]=[CH:40][C:20]3[C:21](=[O:39])[CH2:22][C:23]([CH2:32][CH2:33][C:34]([O:36]CC)=[O:35])([CH2:25][CH2:26][C:27]([O:29]CC)=[O:28])[O:24][C:19]=3[C:18]=2[CH2:42][CH2:43][CH3:44])=[CH:4][CH:3]=1.ClC1C=CC(OCCCOC2C=CC3C(=O)CC(CCC(OCC)=O)(CCC(OCC)=O)OC=3C=2CCC)=CC=1>C(OCC)C>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:13][CH2:14][CH2:15][O:16][C:17]2[CH:41]=[CH:40][C:20]3[C:21](=[O:39])[CH2:22][C:23]([CH2:32][CH2:33][C:34]([OH:36])=[O:35])([CH2:25][CH2:26][C:27]([OH:29])=[O:28])[O:24][C:19]=3[C:18]=2[CH2:42][CH2:43][CH3:44])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 15157438diethyl 3,4-dihydro-7-[3-(4-chlorophenoxy)propoxy]-4-oxo-8-propyl-2H-1-benzopyran-2,2-dipropanoateHCID 15157451diethyl 7-[3-[(4-chloro-1-naphthalenyl)oxy]propoxy]-3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-2,2-dipropanoate

생성물 1

HCID 151574527-[3-[(4-chloro-1-naphthalenyl)oxy]propoxy]-3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-2,2-dipropanoic acid

시약·촉매·용매 1

HCID 3283Diethyl Ether
용매

실험 절차

The title compound was prepared by the method of Example 22 substituting the title product of Example 34 (515 mg) for the title product of Example 21 to give, after trituration with diethylether, 352 mg as a solid, m.p. 170.5°-171° C.

후처리

  1. customto give

출처 및 근거

ORD 기록
ord-056992e92e1f43abbdec47f98d07f01f
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05093353

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