Methyl chloroformate → Methyl {2-[3-({[2-(ethyloxy)ethyl]amino}carbonyl)-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,5-naphthyridine-1(2H)-yl]ethyl}carbamate
반응식
[NH2:1][CH2:2][CH2:3][N:4]1[C:13]2[C:8](=[N:9][CH:10]=[C:11]([CH2:14][C:15]3[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=3)[CH:12]=2)[C:7]([OH:22])=[C:6]([C:23]([NH:25][CH2:26][CH2:27][O:28][CH2:29][CH3:30])=[O:24])[C:5]1=[O:31].C(N(C(C)C)CC)(C)C.Cl[C:42]([O:44][CH3:45])=[O:43]>CN(C=O)C>[CH2:29]([O:28][CH2:27][CH2:26][NH:25][C:23]([C:6]1[C:5](=[O:31])[N:4]([CH2:3][CH2:2][NH:1][C:42](=[O:43])[O:44][CH3:45])[C:13]2[C:8]([C:7]=1[OH:22])=[N:9][CH:10]=[C:11]([CH2:14][C:15]1[CH:16]=[CH:17][C:18]([F:21])=[CH:19][CH:20]=1)[CH:12]=2)=[O:24])[CH3:30]참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
A solution of 1-(2-aminoethyl)-N-[2-(ethyloxy)ethyl]-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide (0.02 g, 0.047 mmol) and diisopropyl ethylamine (0.041 mL, 0.24 mmol) in DMF (5 mL) under nitrogen was treated with methyl chloroformate (0.0036 mL, 0.047 mmol) at ambient temperature. The reaction was concentrated in vacuo and the resulting residue treated with 1 N NaHSO4, filtered, then washed with 1 N NaHSO4 and Et2O before drying in vacuo to provide the title compound as an off-white solid: 1H NMR (300 MHz, DMSO-D6) δ ppm 1.1 (t, J=7.0 Hz, 3 H), 3.3 (m, 2 H), 3.4 (s, 3 H), 3.5 (m, 7 H), 4.1 (s, 2 H), 4.3 (t, J=6.0 Hz, 2 H), 7.1 (t, J=8.8 Hz, 2 H), 7.3 (m, 1 H), 7.4 (m, 2 H), 8.1 (s, 1 H), 8.5 (s, 1 H), 17.1 (s, 1 H); ES+ MS: 487 (M+H+).
후처리
- concentrationThe reaction was concentrated in vacuo
- additionthe resulting residue treated with 1 N NaHSO4
- filtrationfiltered
- washwashed with 1 N NaHSO4 and Et2O
- custombefore drying in vacuo
출처 및 근거
- ORD 기록
- ord-3817395a13bf468db01b8f16dbb822b5
- 출처 데이터셋
- uspto-grants-2014_04
- 특허 번호
- US08691991B2
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