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Diisopropylethylamine → 7-[(3,4-Difluoro-2-methylphenyl)carbonyl]-3-(1,2,4-thiadiazol-5-yl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine

HRID 1889116
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HRID 1889116 반응식
[F:1][C:2]1[C:3]([CH3:12])=[C:4]([CH:8]=[CH:9][C:10]=1[F:11])[C:5]([OH:7])=O.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.[S:46]1[C:50]([C:51]2[N:55]3[CH2:56][CH2:57][NH:58][CH2:59][C:54]3=[N:53][N:52]=2)=[N:49][CH:48]=[N:47]1>CN(C)C=O.C(Cl)Cl>[F:1][C:2]1[C:3]([CH3:12])=[C:4]([C:5]([N:58]2[CH2:57][CH2:56][N:55]3[C:51]([C:50]4[S:46][N:47]=[CH:48][N:49]=4)=[N:52][N:53]=[C:54]3[CH2:59]2)=[O:7])[CH:8]=[CH:9][C:10]=1[F:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 121376783,4-Difluoro-2-methylbenzoic acidHCID 665987953-(1,2,4-Thiadiazol-5-yl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine

생성물 1

HCID 66599041
7-[(3,4-Difluoro-2-methylphenyl)carbonyl]-3-(1,2,4-thiadiazol-5-yl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine

시약·촉매·용매 2

HCID 6228Dimethylformamide용매2회HCID 6344Dichloromethane용매2회

실험 절차

3,4-Difluoro-2-methylbenzoic acid (I68)(124 mg, 0.720 mmol) was dissolved in dry N,N-dimethylformamide (DMF) (4.7 mL) before treating with HATU (274 mg, 0.720 mmol) and DIPEA (0.252 mL, 1.441 mmol) and stirring for 15 mins at RT, under argon before adding 3-(1,2,4-thiadiazol-5-yl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine (I115)(100 mg, 0.480 mmol) and stirring for a further 18 hours. LCMS confirmed that the desired material was present and that no start material was left. The reaction was worked up by diluting with DCM (50 ml), washing with water (50 ml). The aqueous layer was extracted with DCM (2×30 ml). The combined extracts were washed with brine (30 ml), dried (Na2SO4), filtered and evaporated to afford a pale pink gum. The product was purified on a SNAP 50 g cartridge, eluting with 0-10% MeOH in DCM, the desired fractions were collected and the solvent was evaporated to afford a dark orange gum. Due to presence of residual DMF the crude gum product was diluted with DCM (30 ml), washed with brine (2×20 ml), dried (Na2SO4), filtered and evaporated to afford an orange foam. The foam triturated with n-hexane to afford a pale orange solid. Liquers were removed and the residue was triturated again with n-Hexane. Liquers were removed and the solid was dried overnight in the vac oven at 40° C. to afford desired product in 146 mg as a pale orange solid.

후처리

  1. stirringstirring for a further 18 hours
  2. waitwas left
  3. washwashing with water (50 ml)
  4. extractionThe aqueous layer was extracted with DCM (2×30 ml)
  5. washThe combined extracts were washed with brine (30 ml)
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. customevaporated
  9. customto afford a pale pink gum
  10. customThe product was purified on a SNAP 50 g cartridge
  11. washeluting with 0-10% MeOH in DCM
  12. customthe desired fractions were collected
  13. customthe solvent was evaporated
  14. customto afford a dark orange gum
  15. washwashed with brine (2×20 ml)
  16. dry with materialdried (Na2SO4)
  17. filtrationfiltered
  18. customevaporated
  19. customto afford an orange foam
  20. customThe foam triturated with n-hexane
  21. customto afford a pale orange solid
  22. customLiquers were removed
  23. customthe residue was triturated again with n-Hexane
  24. customLiquers were removed
  25. customthe solid was dried overnight in the vac oven at 40° C.

출처 및 근거

ORD 기록
ord-6312d175757f445597e0b16d1c479491
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501946B2

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