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Hydrochloric Acid → HCID 58865792、化合物

HRID 1354837
ノート
印刷プレビュー

反応式

HRID 1354837 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 313Hydrochloric AcidHCID 58865449HCID 58865449、化合物

生成物 1

HCID 58865792HCID 58865792、化合物収率 78.7%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 6422Trifluoroacetic acid溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-2ffc3a3fa6994f93822cfb48141c58f4
出典データセット
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07223759B2

反応ノート

読み込み中…

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