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

Lithium Chloride → HCID 71240815, 화합물

HRID 1774607
노트
인쇄 미리보기

반응식

HRID 1774607 반응식
C[Sn](C)(C)[Sn](C)(C)C.[Cl-].[Li+].Cl[C:12]1[CH:17]=[C:16]([C:18]2[CH:23]=[CH:22][C:21]([O:24][CH:25]([CH3:27])[CH3:26])=[C:20]([Cl:28])[CH:19]=2)[N:15]=[CH:14][N:13]=1.[CH3:29][O:30][C:31]([CH:33]1[CH2:37][C:36](OS(C(F)(F)F)(=O)=O)=[CH:35][N:34]1[C:46]([O:48][C:49]([CH3:52])([CH3:51])[CH3:50])=[O:47])=[O:32]>C1COCC1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Pd]>[CH3:29][O:30][C:31]([CH:33]1[CH2:37][C:36]([C:12]2[CH:17]=[C:16]([C:18]3[CH:23]=[CH:22][C:21]([O:24][CH:25]([CH3:27])[CH3:26])=[C:20]([Cl:28])[CH:19]=3)[N:15]=[CH:14][N:13]=2)=[CH:35][N:34]1[C:46]([O:48][C:49]([CH3:52])([CH3:51])[CH3:50])=[O:47])=[O:32]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 433294Lithium ChlorideHCID 85161366HCID 85161366, 화합물HCID 89396901HCID 89396901, 화합물HCID 178477788HCID 178477788, 화합물

생성물 1

HCID 71240815HCID 71240815, 화합물수율 9%

시약·촉매·용매 2

HCID 11979704
Tetrakis(triphenylphosphine)palladium
촉매
HCID 8028Tetrahydrofuran용매

반응 조건

온도
70 °C

실험 절차

Hexamethyldistannane (5.6 ml, 2.7 mmol) and lithium chloride (0.34 g, 7.8 mmol) were added sequentially in one portion to a stirred solution of, 4-chloro-6-(3-chloro-4-isopropoxy-phenyl)-pyrimidine (0.75 g, 2.7 mmol) and 4-trifluoromethanesulfonyloxy-2,3-dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (1.0 g, 2.7 mmol) in THF (40 ml). The mixture was degassed with nitrogen for 5 minutes, after which time palladium tetrakis(triphenylphosphine) (0.31 g, 0.26 mmol) was added in one portion, the mixture was then heated to 70° C. and stirred at this temperature for 16 hours under a nitrogen atmosphere. After this time the reaction mixture was cooled to room temperature and partitioned between ethyl acetate (200 ml) and saturated potassium fluoride (50 ml). The organic layer was separated, washed sequentially with water (100 ml) then brine (100 ml) before being dried (MgSO4), filtered and concentrated. The resulting red gum was purified by flash column chromatography (elution: 80% EtOAc, 20% Heptane) to give the title compound (0.1 g, 9% yield) as a colourless oil. Tr=2.69 min m/z (ES+) (M+H+) 474.

후처리

  1. customThe mixture was degassed with nitrogen for 5 minutes
  2. temperatureAfter this time the reaction mixture was cooled to room temperature
  3. custompartitioned between ethyl acetate (200 ml) and saturated potassium fluoride (50 ml)
  4. customThe organic layer was separated
  5. washwashed sequentially with water (100 ml)
  6. dry with materialbrine (100 ml) before being dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe resulting red gum was purified by flash column chromatography (elution: 80% EtOAc, 20% Heptane)

출처 및 근거

ORD 기록
ord-bda38543c00c42d784b7db45bbb755c1
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09260422B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트