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HCID 67168853, 화합물 → Methyl 2-((3S,4S)-4-(aminomethyl)-1-methylpyrrolidin-3-yl)-6-(trifluoromethoxy)benzoate

HRID 84947
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HRID 84947 반응식
[C:1]([C@H:3]1[CH2:7][N:6]([CH3:8])[CH2:5][C@@H:4]1[C:9]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19][C:20]([F:23])([F:22])[F:21])[C:10]=1[C:11]([O:13][CH3:14])=[O:12])#[N:2].C(N1C[C@@H](C#N)[C@H](C2C=CC(Cl)=CC=2C(OC)=O)C1)C1C=CC=CC=1>>[NH2:2][CH2:1][C@H:3]1[CH2:7][N:6]([CH3:8])[CH2:5][C@@H:4]1[C:9]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19][C:20]([F:23])([F:21])[F:22])[C:10]=1[C:11]([O:13][CH3:14])=[O:12]
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3

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HCID 67168853HCID 67168853, 화합물HCID 131731904HCID 131731904, 화합물

생성물 1

HCID 67168219Methyl 2-((3S,4S)-4-(aminomethyl)-1-methylpyrrolidin-3-yl)-6-(trifluoromethoxy)benzoate

실험 절차

The title compound was prepared according to the procedure outlined in Example 45C substituting the product obtained from Example 110A for the product obtained from Example 45B. In this instance, the aminoester did not cyclize. 1H NMR (300 MHz, DMSO-d6) δ ppm 1.42 (s, 1H) 2.10-2.21 (m, 1H) 2.32-2.48 (m, 4H) 2.55-2.63 (m, 1H) 2.73 (t, J=8.48 Hz, 1H) 2.79-2.87 (m, 3H) 3.87 (s, 3H) 7.28-7.36 (m, 1H) 7.55-7.64 (m, 3H); MS (DCI+) m/z 333.2 [M+H]+.

출처 및 근거

ORD 기록
ord-ae95f29bbc3b40f894d3828d0b594a87
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846951B2

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