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2-(3-Nitro-6-propylaminophenyl)-5-(4-chlorophenyl)benzoxazole → 2-(3-Amino-6-propylaminophenyl)-5-(4-chlorophenyl)benzoxazole

HRID 722664
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인쇄 미리보기

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HRID 722664 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([C:14]2[O:15][C:16]3[CH:22]=[CH:21][C:20]([C:23]4[CH:28]=[CH:27][C:26]([Cl:29])=[CH:25][CH:24]=4)=[CH:19][C:17]=3[N:18]=2)[C:7]([NH:10][CH2:11][CH2:12][CH3:13])=[CH:8][CH:9]=1)([O-])=O>[Zn]>[NH2:1][C:4]1[CH:5]=[C:6]([C:14]2[O:15][C:16]3[CH:22]=[CH:21][C:20]([C:23]4[CH:28]=[CH:27][C:26]([Cl:29])=[CH:25][CH:24]=4)=[CH:19][C:17]=3[N:18]=2)[C:7]([NH:10][CH2:11][CH2:12][CH3:13])=[CH:8][CH:9]=1
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참가 물질

3

반응물 1

HCID 218843402-(3-Nitro-6-propylaminophenyl)-5-(4-chlorophenyl)benzoxazole

생성물 1

HCID 218844412-(3-Amino-6-propylaminophenyl)-5-(4-chlorophenyl)benzoxazole

시약·촉매·용매 1

HCID 23994Zinc촉매

실험 절차

Prepared by the method of Example 47b), from 2-(3-nitro-6-propylaminophenyl)-5-(4-chlorophenyl)benzoxazole (284 mg, 0.70 mmol) and zinc (455 mg, 7.0 mmol) the subtitle compound was obtained (264 mg, 99%). The product was used directly in the next step without purification

출처 및 근거

ORD 기록
ord-c5342dff12274d64a220f4e8956683c3
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07138425B2

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