Hydrochloric Acid → HCID 178502474, 화합물

HRID 1751617노트

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HRID 1751617 반응식
Cl.[O:2]1[CH2:7][CH2:6]OCC1.[CH3:8][O:9][C:10]([NH:12][C@@H:13]([CH:61]([CH3:63])[CH3:62])[C:14]([N:16]1[C@H:21]([C:22]2[NH:26][C:25]3[C:27]4[C:32]([CH:33]=[CH:34][C:24]=3[N:23]=2)=[CH:31][C:30]([C:35]2[CH:36]=[C:37]3[C:57](=[CH:58][CH:59]=2)[C:41]2[NH:42][C:43]([C@@H:45]5[CH2:49][CH2:48][CH2:47][N:46]5C(OC(C)(C)C)=O)=[N:44][C:40]=2[CH:39]=[CH:38]3)=[CH:29][CH:28]=4)[C@H:20]2[CH2:60][C@@H:17]1[CH2:18][CH2:19]2)=[O:15])=[O:11].COC(N[C@H]([C:73]1[CH:78]=[CH:77][CH:76]=[CH:75][CH:74]=1)C(O)=O)=O.CC[N:81](C(C)C)C(C)C.C[CH2:89][O:90][C:91](C(C#N)=NOC(N1CCOCC1)=[N+](C)C)=[O:92].F[P-](F)(F)(F)(F)F>C(Cl)Cl.CN(C=O)C.CO>[CH3:8][O:9][C:10]([NH:12][C@@H:13]([CH:61]([CH3:62])[CH3:63])[C:14]([N:16]1[C@H:21]([C:22]2[NH:26][C:25]3[C:27]4[C:32]([CH:33]=[CH:34][C:24]=3[N:23]=2)=[CH:31][C:30]([C:35]2[CH:36]=[C:37]3[C:57](=[CH:58][CH:59]=2)[C:41]2[NH:42][C:43]([C@@H:45]5[CH2:49][CH2:48][CH2:47][N:46]5[C:7](=[O:2])[C@H:6]([NH:81][C:91](=[O:92])[O:90][CH3:89])[C:76]5[CH:75]=[CH:74][CH:73]=[CH:78][CH:77]=5)=[N:44][C:40]=2[CH:39]=[CH:38]3)=[CH:29][CH:28]=4)[C@H:20]2[CH2:60][C@@H:17]1[CH2:18][CH2:19]2)=[O:15])=[O:11]

참가 물질

10

반응물 6

HCID 313Hydrochloric AcidHCID 312751,4-DioxaneHCID 81531DiisopropylethylamineHCID 10910775(alphaR)-alpha-((Methoxycarbonyl)amino)benzeneacetic acidHCID 75951468(1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphateHCID 178502475HCID 178502475, 화합물

생성물 1

HCID 178502474HCID 178502474, 화합물수율 53%

시약·촉매·용매 3

HCID 887Methanol용매HCID 6228Dimethylformamide용매HCID 6344Dichloromethane용매2회

실험 절차

Hydrogen chloride in dioxane solution (4N, 1.51 mL, 6.05 mmol) was added to a solution of (S)-tert-butyl 2-(2′-((1S,3S,4R)-2-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-2-azabicyclo[2.2.1]heptan-3-yl)-1H,1′H-7,7′-binaphtho[1,2-d]imidazol-2-yl)pyrrolidine-1-carboxylate (0.305 g, 0.403 mmol) in methylene chloride:methanol (4.0 mL: 0.80 mL). The suspension was allowed to stir at room temperature for two hours. Upon completion by LCMS, the reaction was concentrated to dryness and the crude product (assumed 0.403 mmol) was suspended in methylene chloride (4 mL). (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (0.093 g, 0.484 mmol) and DIPEA (0.282 mL, 1.61 mmol) were added and the slurry was cooled to −40° C. with an external dry ice/acetonitrile bath. COMU (0.259 g, 0.605 mmol) was added at −40° C. and the solution was stirred at reduced temperature for one hour. Upon completion, the crude reaction was diluted with DMF and concentrated in vacuo. The crude product was purified by reverse phase HPLC (Gilson, Gemini, 10-45% acetonitrile/water with 0.1% TFA modifier). Fractions containing product were combined and concentrated until aqueous layer remained. Aqueous sodium bicarbonate was added to aqueous product mixture to obtain a pH of 7-8 (as measured by pH paper) and precipitation was observed. The precipitate was filtered and dried under vacuum for 18 hours to give methyl {(1R)-2-[(2S)-2-{2′-[(1S,3S,4R)-2-{(2S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl}-2-azabicyclo[2.2.1]hept-3-yl]-1H,1′H-7,7′-binaphtho[1,2-d]imidazol-2-yl}pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (0.180 g, 53%) as a while solid. LCMS-ESI+: calc'd for C49H50N8O6: 846.39 (M+); Found: 847.8 (M+H+).

후처리

  1. concentrationUpon completion by LCMS, the reaction was concentrated to dryness
  2. temperaturethe slurry was cooled to −40° C. with an external dry ice/acetonitrile bath
  3. stirringthe solution was stirred at reduced temperature for one hour
  4. customUpon completion, the crude reaction
  5. concentrationconcentrated in vacuo
  6. customThe crude product was purified by reverse phase HPLC (Gilson, Gemini, 10-45% acetonitrile/water with 0.1% TFA modifier)
  7. additionFractions containing product
  8. concentrationconcentrated until aqueous layer
  9. additionAqueous sodium bicarbonate was added to aqueous product mixture
  10. customto obtain
  11. customa pH of 7-8 (as measured by pH paper) and precipitation
  12. filtrationThe precipitate was filtered
  13. customdried under vacuum for 18 hours

출처 및 근거

ORD 기록
ord-6fc423cd22b34c0a8a2809a180312883
출처 데이터셋
uspto-grants-2015_10
특허 번호
US09156823B2

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