Triethylamine → 2-(4-Methoxy-2,3,6-trimethyl-benzenesulfonylamino)-3-phenyl-propionic acid methyl ester
반응식
[CH3:1][O:2][C:3](=[O:13])[C@H:4]([CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[NH2:5].C(N(CC)CC)C.[CH3:21][O:22][C:23]1[CH:28]=[C:27]([CH3:29])[C:26]([S:30](Cl)(=[O:32])=[O:31])=[C:25]([CH3:34])[C:24]=1[CH3:35]>C(Cl)Cl.CN(C1C=CN=CC=1)C>[CH3:1][O:2][C:3](=[O:13])[CH:4]([NH:5][S:30]([C:26]1[C:27]([CH3:29])=[CH:28][C:23]([O:22][CH3:21])=[C:24]([CH3:35])[C:25]=1[CH3:34])(=[O:32])=[O:31])[CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
A solution of L-phenylalanine methyl ester (300 mg, 1.68 mmol) in anhydrous CH2Cl2 (10 mL) was cooled to 0° C. in an ice bath, then triethylamine (0.35 mL), 4-methoxy-2,3,6-trimethyl-benzenesulfonyl chloride (438 mg, 1.76 mmol) and catalytic amount of DMAP (25 mg) were added under a N2 atmosphere. The reaction mixture was stirred at room temperature for 12 h. After that period of time, the mixture was partitioned between water and CH2Cl2, the organic layer was separated, dried (Na2SO4) and concentrated. The residue was purified by silica gel column chromatography using ethyl acetate and hexane (1:2) as eluent to obtain 2-(4-Methoxy-2,3,6-trimethyl-benzenesulfonylamino)-3-phenyl-propionic acid methyl ester as a white solid, 500 mg (77%). 1H NMR (CDCl3, 400 MHz): δ7.26-7.18 (m, 3H), 7.02-6.99 (m, 2H), 6.53 (s, 1H), 5.12 (d, 1H), 4.09-4.04 (m, 1H), 3.84 (s, 3H), 3.55 (s, 3H), 3.05 (dd, 1H), 3.03 (dd, 1H), 2.64, 2.38, 2.08 (3s, 9H).
후처리
- waitAfter that period of time
- customthe mixture was partitioned between water and CH2Cl2
- customthe organic layer was separated
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- customThe residue was purified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-db201fb0ba5c48e3831ed0446dc452e2
- 출처 데이터셋
- uspto-grants-2005_05
- 특허 번호
- US06887877B2
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