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HCID 178445744, 화합물 → HCID 178447443, 화합물

HRID 1036470
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HRID 1036470 반응식
C([C@H]1CC[C@H](OC2C(C(F)(F)F)=C3C(=CC=2)C=C(C([N+]([O-])=O)CCC(O)=O)C=C3)CC1)(C)(C)C.[C:35]([C@H:39]1[CH2:44][CH2:43][C@H:42]([O:45][C:46]2[CH:47]=[C:48]3[C:53](=[CH:54][CH:55]=2)[CH:52]=[C:51]([C:56]([N+:64]([O-:66])=[O:65])([CH3:63])[CH2:57][CH2:58][C:59]([O:61]C)=[O:60])[CH:50]=[CH:49]3)[CH2:41][CH2:40]1)([CH3:38])([CH3:37])[CH3:36]>>[C:35]([C@H:39]1[CH2:40][CH2:41][C@H:42]([O:45][C:46]2[CH:47]=[C:48]3[C:53](=[CH:54][CH:55]=2)[CH:52]=[C:51]([C:56]([N+:64]([O-:66])=[O:65])([CH3:63])[CH2:57][CH2:58][C:59]([OH:61])=[O:60])[CH:50]=[CH:49]3)[CH2:43][CH2:44]1)([CH3:38])([CH3:36])[CH3:37]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 178445744HCID 178445744, 화합물HCID 178500163HCID 178500163, 화합물

생성물 1

HCID 178447443HCID 178447443, 화합물수율 96%

실험 절차

4-(6-(trans-4-tert-butylcyclohexyloxy)naphthalen-2-yl)-4-nitropentanoic acid was synthesized as per 4-(6-(trans-4-tert-butylcyclohexyloxy)-5-(trifluoromethyl)naphthalen-2-yl)-4-nitrobutanoic acid (Example 202) in 96% yield using methyl 4-(6-(trans-4-tert-butylcyclohexyloxy)naphthalen-2-yl)-4-nitropentanoate as starting material.

출처 및 근거

ORD 기록
ord-6722c165f18a409ca4065d3743b5e2a7
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08546359B2

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