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3-Chloro-4-(3-fluorobenzyloxy)aniline → HCID 57597277, 화합물

HRID 1786888
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인쇄 미리보기

반응식

HRID 1786888 반응식
Cl[C:2]1[C:3]2[N:10]([CH2:11][CH3:12])[CH:9]=[CH:8][C:4]=2[N:5]=[CH:6][N:7]=1.[Cl:13][C:14]1[CH:15]=[C:16]([CH:18]=[CH:19][C:20]=1[O:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([F:29])[CH:24]=1)[NH2:17]>CN1CCCC1=O>[Cl:13][C:14]1[CH:15]=[C:16]([NH:17][C:2]2[C:3]3[N:10]([CH2:11][CH3:12])[CH:9]=[CH:8][C:4]=3[N:5]=[CH:6][N:7]=2)[CH:18]=[CH:19][C:20]=1[O:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([F:29])[CH:24]=1
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참가 물질

4

반응물 2

HCID 70592633-Chloro-4-(3-fluorobenzyloxy)anilineHCID 714134604-Chloro-5-ethyl-5H-pyrrolo[3,2-d]pyrimidine

생성물 1

HCID 57597277HCID 57597277, 화합물수율 52.8%

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매

실험 절차

To a solution of 4-chloro-5-ethyl-5H-pyrrolo[3,2-d]pyrimidine (85 mg) in 1-methyl-2-pyrrolidone (0.94 mL) was added 3-chloro-4-[(3-fluorobenzyl)oxy]aniline (177 mg). The title compound (98 mg) was obtained as a pale-purple powder crystals by the reaction in the same manner as in Example 29.

출처 및 근거

ORD 기록
ord-c3865050c042497a812c2daf532247a2
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07507740B2

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