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Hydrochloric Acid → HCID 69422026、化合物

HRID 1354838
ノート
印刷プレビュー

反応式

HRID 1354838 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]([N+:55]([O-])=O)[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]([NH2:55])[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 58865534HCID 58865534、化合物

生成物 1

HCID 69422026HCID 69422026、化合物収率 31.1%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 6422Trifluoroacetic acid溶媒

実験手順

2,3-Bis-((3R,5S)-3,5-bis-(tert-Butoxycarbonylamino)-piperidin-1-yl)-6-nitro-quinoxaline (245) (0.05 g, 0.135 mmol) was dissolved in TFA (3 mL) and the mixture was shaken at room temperature in a Teflon septum capped vial 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 (255) as an orange powder (0.023 g, 0.042 mmol, 31% yield, assumed 4 HCl salt). LC-MS (ESI): (exact mass: 401.23) m/e=402.2 [M+1]+. 1H NMR (400 MHz, D2O): δ 1.72 (q, 2H, J=12 Hz), 2.49 (d, 2H, J=10 Hz), 2.94 (q, 4H, J=12 Hz), 3.51–3.67 (m, 4H), 4.44 (dd, 2H, J1=12 Hz, J2=4.4 Hz), 4.57 (dd, 2H, J1=12.8 Hz, J2=3.6 Hz), 7.71 (d, 1H, J=9.2 Hz), 8.10 (dd, 1H, J1=9.2 Hz, J2=2.8 Hz), 8.44 (d, 1H, J=2.4 Hz).

後処理

  1. customcapped vial 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-3f40b13288d24493a712b6ededdbdf2a
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…

このページの内容参加物実験手順後処理出典と根拠反応ノート