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Hydrochloric Acid → HCID 58865792, 화합물

HRID 1354837
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HRID 1354837 반응식
C(OC([NH:8][C@@H:9]1[CH2:14][C@H:13]([NH:15]C(OC(C)(C)C)=O)[CH2:12][N:11]([C:23]2[C:32]([N:33]3[CH2:38][C@@H:37]([NH:39]C(OC(C)(C)C)=O)[CH2:36][C@@H:35]([NH:47]C(OC(C)(C)C)=O)[CH2:34]3)=[N:31][C:30]3[C:25](=[CH:26][CH:27]=[C:28]([NH:55][C:56]([C:58]4[CH:63]=[CH:62][C:61]([NH:64][C:65]([C:67]5[CH:76]=[CH:75][C:74]6[C:69](=[CH:70][CH:71]=[CH:72][CH:73]=6)[C:68]=5[OH:77])=[O:66])=[CH:60][CH:59]=4)=[O:57])[CH:29]=3)[N:24]=2)[CH2:10]1)=O)(C)(C)C.Cl>C(O)(C(F)(F)F)=O.CO>[NH2:15][C@@H:13]1[CH2:14][C@H:9]([NH2:8])[CH2:10][N:11]([C:23]2[C:32]([N:33]3[CH2:34][C@@H:35]([NH2:47])[CH2:36][C@@H:37]([NH2:39])[CH2:38]3)=[N:31][C:30]3[C:25](=[CH:26][CH:27]=[C:28]([NH:55][C:56]([C:58]4[CH:63]=[CH:62][C:61]([NH:64][C:65]([C:67]5[CH:76]=[CH:75][C:74]6[C:69](=[CH:70][CH:71]=[CH:72][CH:73]=6)[C:68]=5[OH:77])=[O:66])=[CH:60][CH:59]=4)=[O:57])[CH:29]=3)[N:24]=2)[CH2:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 58865449HCID 58865449, 화합물

생성물 1

HCID 58865792HCID 58865792, 화합물수율 78.7%

시약·촉매·용매 2

HCID 887Methanol용매HCID 6422Trifluoroacetic acid용매

실험 절차

1-Hydroxy-naphthalene-2-carboxylic acid [4-(2,3-bis-((3R,5S)-3,5-bis-(tert-Butoxycarbonylamino)-piperidin-1-yl)-quinoxalin-6-ylcarbamoyl)-phenyl]-amide (253) (9 mg, 8.5 μmmol) was dissolved in TFA (1 mL) and the mixture was shaken in a Teflon septum capped vial at room temperature for 3 hours. LC-MS indicated complete de-protection at this point. The solution was concentrated to give an orange oil. The oil was dissolved in MeOH (1 mL) and HCl (1 mL, 4.0 M in dioxane) was added and the mixture was vortexed for 20 seconds. A fine suspension was observed. The mixture was concentrated to an orange powder. Ethyl ether (5 mL) was added to the powder and vortexed for 2 minutes. The solid was collected by filtration and dried under high vacuum for 16 hours to give the desired product (254) as a yellow/green powder (5.4 mg, 6.69 μmmol, 78.7% yield, assuming a 4 HCl salt). LC-MS (ESI): (exact mass: 660.33) m/e=661.6 [M+1]+. 1H NMR (400 MHz, D2O): δ 1.70–1.82 (m, 2H), 2.61–2.65 (m, 2H), 2.78–2.94 (m, 2H), 3.57–3.60 (m, 2H), 3.67–3.68 (m, 4H), 3.97 (d, 2H, J=9.6 Hz), 4.23 (d, 2H, J=9.6 Hz), 6.89 (d, 1H, J=8.8 Hz), 7.14 (d, 1H, J=8.4 Hz), 7.18–7.29 (m, 3H), 7.32–7.53 (m, 6H), 7.74 (d, 2H, J=7.6 Hz).

후처리

  1. customcapped vial at room temperature for 3 hours
  2. concentrationThe solution was concentrated
  3. customto give an orange oil
  4. concentrationThe mixture was concentrated to an orange powder
  5. additionEthyl ether (5 mL) was added to the powder
  6. waitvortexed for 2 minutes
  7. filtrationThe solid was collected by filtration
  8. customdried under high vacuum for 16 hours

출처 및 근거

ORD 기록
ord-2ffc3a3fa6994f93822cfb48141c58f4
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07223759B2

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