Hydrochloric Acid → 3-(6-[N,N-bis(tert-butoxycarbonyl)amino]-5-methyl-pyridin-3-yl)-2-hydroxymethyl-2-methyl-propionic acid ethyl ester
반응식
ClC(OC)=O.[CH2:6]([O:8][C:9](=[O:38])[C:10]([CH2:15][C:16]1[CH:17]=[N:18][C:19]([N:23]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])=[C:20]([CH3:22])[CH:21]=1)([CH3:14])[C:11](O)=[O:12])[CH3:7].CCN(CC)CC.[BH4-].[Na+].Cl>C1COCC1.C(Cl)Cl>[CH2:6]([O:8][C:9](=[O:38])[C:10]([CH2:11][OH:12])([CH3:14])[CH2:15][C:16]1[CH:17]=[N:18][C:19]([N:23]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])=[C:20]([CH3:22])[CH:21]=1)[CH3:7]참가 물질
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
Methyl chloroformate (338 μL, 4.4 mmol) was added dropwise to a solution of crude 2-(6-[N,N-bis(tert-butoxycarbonyl)amino]-5-methyl-pyridin-3-yl methyl)-2-methyl-malonic acid monoethyl ester (1.9 g) and Et3N (641 μL, 4.6 mmol) in THF (30 mL) at −20° C. The reaction mixture was stirred for 50 min., filtered and added dropwise to a suspension of NaBH4 (182 mg, 4.8 mmol) in THF (30 mL) at −20° C. The reaction was stirred for 16 h at room temperature. 0.5 M HCl was added followed by methylene chloride. The organic phase was washed with brine and dried. Concentration under reduced pressure followed by chromathography (toluene/EtOAc, 10:1→1:3) gave 3-(6-[N,N-bis(tert-butoxycarbonyl)-amino]-5-methyl-pyridin-3-yl)-2-hydroxymethyl-2-methyl-propionic acid ethyl ester (885 mg, 49%).
후처리
- filtrationfiltered
- stirringThe reaction was stirred for 16 h at room temperature
- washThe organic phase was washed with brine
- customdried
- concentrationConcentration under reduced pressure
출처 및 근거
- ORD 기록
- ord-b2cf4b90866342179f06cdfb89ca06a9
- 출처 데이터셋
- uspto-grants-2006_07
- 특허 번호
- US07071175B1
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