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2,4-Dichloropyrimidine → HCID 57428832, 화합물

HRID 507573
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HRID 507573 반응식
[Li]CCCC.[CH3:6][Si:7]([CH3:14])([CH3:13])[C:8]1[S:9][CH:10]=[CH:11][CH:12]=1.[Cl:15][C:16]1[N:21]=[C:20](Cl)[CH:19]=[CH:18][N:17]=1>C1COCC1.CCOCC.[Cl-].[Cl-].[Zn+2].C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Cl:15][C:16]1[N:21]=[C:20]([C:10]2[S:9][C:8]([Si:7]([CH3:14])([CH3:13])[CH3:6])=[CH:12][CH:11]=2)[CH:19]=[CH:18][N:17]=1
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참가 물질

8

반응물 3

HCID 775312,4-DichloropyrimidineHCID 140360Silane, trimethyl-2-thienyl-HCID 178418339Butyllithium

생성물 1

HCID 57428832HCID 57428832, 화합물

시약·촉매·용매 4

HCID 3007855Zincchloride촉매HCID 178418397HCID 178418397, 화합물
촉매
HCID 3283Diethyl Ether용매
HCID 8028Tetrahydrofuran용매3회

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온도
-78 °C

실험 절차

nBuLi (1.9 mL, 1.6 M solution in hexane, 3.0 mmol) was added to a stirred solution of 0.50 mL (3.0 mmol) of 2-(trimethylsilyl)thiophene in 7 mL of THF at −78° C. The solution was stirred for 30 min at −78° C., then warmed to 0° C. and stirred 30 min, before 6.1 mL (3.0 mmol) of a 0.5 M solution of ZnCl2 in THF was added. The reaction solution was stirred for 30 min at 0° C., then transferred via syringe to a microwave vessel containing 315 mg (2.8 mmol) of 2,4-dichloropyrimidine and 158 mg (0.14 mmol) of tetrakis(triphenylphosphine)palladium(0) in 2 mL of THF. The vessel was sealed and heated in a microwave for 10 min at 160° C., then cooled to rt, diluted with 100 mL of Et2O, dried over MgSO4, filtered, concentrated in vacuo, and purified by flash chromatography eluting with a linear gradient of 20% EtOAc in hexane to 50% EtOAc to deliver the title compound. MS (M+H)+ 269.

후처리

  1. temperaturewarmed to 0° C.
  2. additionwas added
  3. stirringThe reaction solution was stirred for 30 min at 0° C.
  4. customtransferred via syringe to a microwave vessel
  5. customThe vessel was sealed
  6. temperatureheated in a microwave for 10 min at 160° C.
  7. temperaturecooled to rt
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. custompurified by flash chromatography
  12. washeluting with a linear gradient of 20% EtOAc in hexane to 50% EtOAc

출처 및 근거

ORD 기록
ord-ea4b1ea49598435cbe40cd4336373cc4
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07786132B2

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