홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Ammonium Chloride → (R)-3-(6-bromo-3-fluoro-4-triethylsilanyl-pyridin-2-yl)-2,2-difluoro-3-((R)-2-methyl-propane-2-sulfinylamino)-butyric acid ethyl ester

HRID 1752456
노트
인쇄 미리보기

반응식

HRID 1752456 반응식
Br[C:2]([F:9])([F:8])[C:3]([O:5][CH2:6][CH3:7])=[O:4].[Br:10][C:11]1[N:16]=[C:15](/[C:17](=[N:19]/[S@@:20]([C:22]([CH3:25])([CH3:24])[CH3:23])=[O:21])/[CH3:18])[C:14]([F:26])=[C:13]([Si:27]([CH2:32][CH3:33])([CH2:30][CH3:31])[CH2:28][CH3:29])[CH:12]=1.[Cl-].[NH4+]>C1COCC1.C[Si](C)(C)Cl.C(OCC)(=O)C.[Zn].[Cu]Cl>[CH2:6]([O:5][C:3](=[O:4])[C:2]([F:9])([F:8])[C@@:17]([C:15]1[C:14]([F:26])=[C:13]([Si:27]([CH2:30][CH3:31])([CH2:28][CH3:29])[CH2:32][CH3:33])[CH:12]=[C:11]([Br:10])[N:16]=1)([NH:19][S@@:20]([C:22]([CH3:23])([CH3:24])[CH3:25])=[O:21])[CH3:18])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 3

HCID 25517Ammonium ChlorideHCID 69585Ethyl bromodifluoroacetateHCID 89415106(NE,R)-N-[1-(6-bromo-3-fluoro-4-triethylsilyl-2-pyridinyl)ethylidene]-2-methylpropane-2-sulfinamide

생성물 1

HCID 86689143(R)-3-(6-bromo-3-fluoro-4-triethylsilanyl-pyridin-2-yl)-2,2-difluoro-3-((R)-2-methyl-propane-2-sulfinylamino)-butyric acid ethyl ester수율 77%

시약·촉매·용매 5

HCID 6397
Chlorotrimethylsilane
촉매
HCID 23994Zinc촉매2회
HCID 62652Cuprous chloride촉매
HCID 8028Tetrahydrofuran용매2회
HCID 8857Ethyl Acetate용매

실험 절차

To a suspension of zinc (466 mg, 7.12 mmol) and copper(I) chloride (34 mg, 0.344 mmol) in dry THF (20 ml) were added 3 drops of trimethylchlorosilane under nitrogen to activate the zinc. After 10 minutes ethyl 2-bromo-2,2-difluoroacetate (1.398 g, 6.89 mmol) was added slowly by syringe over a period of 10 minutes at 25° C. (slightly exothermic). The reaction mixture was kept in an ultrasound bath for 45 minutes. This black fine suspension was added dropwise to a solution of (R)-2-methyl-propane-2-sulfinic acid [1-(6-bromo-3-fluoro-4-triethylsilanyl-pyridin-2-yl)-eth-(E)-ylidene]-amide) (1 g, 2.296 mmol) in dry THF (10 ml) at it under inert atmosphere. After 4 h at it the reaction mixture was added to a cold aq. ammonium chloride solution (5%) and was diluted with ethyl acetate. The organic phase was washed with aq. citric acid (5% solution), water, sat. sodium bicarbonate solution and brine, dried over sodium sulfate, filtered and concentrated. The crude brownish oil (1.5 g) was chromatographed over silica gel (cyclohexane/ethyl acetate 83:17) to give the title compound as a light yellow oil. 984 mg (77% yield).

후처리

  1. washThe organic phase was washed with aq. citric acid (5% solution), water, sat. sodium bicarbonate solution and brine
  2. dry with materialdried over sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe crude brownish oil (1.5 g) was chromatographed over silica gel (cyclohexane/ethyl acetate 83:17)

출처 및 근거

ORD 기록
ord-6de3b259cf004013b8fb25f07fff9a97
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09163011B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트