Triethylamine → N-(tert-butyl)-N'-[(1R)-2-hydroxy-1-(3-pyridylmethyl)ethyl]thiourea

HRID 1280595

반응식

HRID 1280595 반응식
C(N(CC)CC)C.[C:8]([N:12]=[C:13]=[S:14])([CH3:11])([CH3:10])[CH3:9].Cl.Cl.[NH2:17][C@H:18]([CH2:21][C:22]1[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=1)[CH2:19][OH:20]>C(O)C.C(OCC)(=O)C.O.ClCCl>[C:8]([NH:12][C:13]([NH:17][C@H:18]([CH2:21][C:22]1[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=1)[CH2:19][OH:20])=[S:14])([CH3:11])([CH3:10])[CH3:9]

참가 물질

8

반응물 3

HCID 8471TriethylamineHCID 11544tert-Butyl isothiocyanateHCID 69885129(2R)-2-amino-3-(3-pyridyl)-1-propanol dihydrochloride

생성물 1

HCID 86584417N-(tert-butyl)-N'-[(1R)-2-hydroxy-1-(3-pyridylmethyl)ethyl]thiourea

시약·촉매·용매 4

HCID 702Ethanol용매HCID 962Water용매HCID 6344Dichloromethane용매HCID 8857Ethyl Acetate용매

반응 조건

온도
60 °C

실험 절차

22.7 cm3 of triethylamine and then 14 cm3 of tert-butyl isothiocyanate are added dropwise to a suspension, under an inert atmosphere, of 16.51 g of (2R)-2-amino-3-(3-pyridyl)-1-propanol dihydrochloride in 200 cm3 of ethanol. The mixture is then heated at a temperature in the region of 60° C. for 1 hour 30 min. After cooling to a temperature in the region of 20° C., the insoluble material is filtered off on a sinter funnel and the filtrate is then evaporated under reduced pressure (2 kPa) at a temperature in the region of 40° C. A yellow paste is obtained, and is taken up in 200 cm3 of ethyl acetate and 100 cm3 of water. The aqueous phase is extracted and then washed with twice 200 cm3 of ethyl acetate. The organic phases are combined, washed with 3 times 50 cm3 of saturated sodium chloride solution and dried over magnesium sulfate. After filtration and then evaporation under reduced pressure (2 kPa) at a temperature in the region of 40° C., a yellow oil is obtained, which is taken up in dichloromethane and re-evaporated to give 3.25 g of N-(tert-butyl)-N′-[(1R)-2-hydroxy-1-(3-pyridylmethyl)-ethyl]thiourea in the form of a pale yellow foam: [1H NMR spectrum (400 MHz, (CD3)2SO-d6, δ in ppm): 1.41 (s: 9H); 2.84 (mt: 2H); 3.37 (mt: 2H); 4.43 (unres. mult.: 1H); 4.96 (t, J=5 Hz: 1H); 7.24 (d, J=8 Hz: 1H); 7.27 (broad S: 1H); 7.33 (dd, J=8 and 5 Hz: 1H); 7.67 (dt, J=8 and 2 Hz: 1H); 8.42 (dd, J=5 and 2 Hz: 1H); 8.46 (d, J=2 Hz: 1H)].

후처리

  1. temperatureAfter cooling to a temperature in the region of 20° C.
  2. filtrationthe insoluble material is filtered off on a sinter funnel
  3. customthe filtrate is then evaporated under reduced pressure (2 kPa) at a temperature in the region of 40° C
  4. customA yellow paste is obtained
  5. extractionThe aqueous phase is extracted
  6. washwashed with twice 200 cm3 of ethyl acetate
  7. washwashed with 3 times 50 cm3 of saturated sodium chloride solution
  8. dry with materialdried over magnesium sulfate
  9. filtrationAfter filtration
  10. customevaporation under reduced pressure (2 kPa) at a temperature in the region of 40° C.
  11. customa yellow oil is obtained
  12. customre-evaporated

출처 및 근거

ORD 기록
ord-7f912e4c0c884a7d97c773e6a35f6ab9
출처 데이터셋
uspto-grants-2002_09
특허 번호
US06451821B1

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