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Hydrochloric Acid → HCID 178447013、化合物

HRID 511684
ノート
印刷プレビュー

反応式

HRID 511684 の反応式
[CH3:1][O:2][CH2:3][C:4]([C:7]1[CH:44]=[CH:43][C:10]2[NH:11][C:12]([CH2:14][CH2:15][CH:16]3[CH2:19][CH:18]([N:20]([CH2:22][C@@H:23]4[C@H:27]5[O:28]C(C)(C)[O:30][C@H:26]5[C@H:25]([N:33]5[CH:41]=[N:40][C:39]6[C:34]5=[N:35][CH:36]=[N:37][C:38]=6[NH2:42])[O:24]4)[CH3:21])[CH2:17]3)=[N:13][C:9]=2[CH:8]=1)([CH3:6])[CH3:5].Cl.[CH3:46]O>>[NH2:42][C:38]1[N:37]=[CH:36][N:35]=[C:34]2[C:39]=1[N:40]=[CH:41][N:33]2[C@H:25]1[C@H:26]([OH:30])[C@H:27]([OH:28])[C@@H:23]([CH2:22][N:20]([CH:18]2[CH2:19][CH:16]([CH2:15][CH2:14][C:12]3[NH:11][C:10]4[CH:43]=[CH:44][C:7]([C:4]([CH2:5][CH3:46])([CH3:6])[CH2:3][O:2][CH3:1])=[CH:8][C:9]=4[N:13]=3)[CH2:17]2)[CH3:21])[O:24]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 178494914HCID 178494914、化合物

生成物 1

HCID 178447013HCID 178447013、化合物収率 53%

実験手順

9-[(3aR,4R,6R,6aR)-6-{[(3-{2-[5-(1-Methoxy-2-methylpropan-2-yl)-1H-1,3-benzodiazol-2-yl]ethyl}cyclobutyl)(methyl)amino]methyl}-2,2-dimethyl-tetrahydro-2H-furo[3,4-d][1,3]dioxol-4-yl]-9H-purin-6-amine (0.485 g, 0.706 mmol, 88% pure) was dissolved in MeOH (20 ml) and conc. HCl (4.9 ml, 10 vol) was added at r.t. and the reaction left for 2.5 h. The reaction was concentrated in vacuo and the residue dissolved in the minimum amount of MeOH (˜2 ml). The reaction was quenched by addition of sat. NaHCO3 solution (10 ml) and EtOAc (30 ml). The layers were separated and the aqueous layer was extracted with EtOAc (2×30 ml). The combined organic layers were dried over MgSO4, filtered and concentrated in vacuo to give the crude product. The product was purified by silica flash column chromatography using between 100% DCM and 20% 2M NH3 in MeOH:80% DCM as eluent to give the product as a white foam (0.213 g, 53%): MS (ESI+) for C29H40N8O4 m/z 565.4 [M+H]+; LC purity 100% (ret. time, 2.11 min) (7 min); 1H NMR (500 MHz, d4-MeOD) δH 8.28 (d, J=4.1 Hz, 1H), 8.22 (d, J=3.2 Hz, 1H), 7.51 (s, 1H), 7.42 (dd, J=8.5, 2.1 Hz, 1H), 7.29 (dd, J=8.5, 1.5 Hz, 1H), 6.01 (t, J=3.9 Hz, 1H), 4.84-4.74 (m, 1H), 4.41-4.29 (m, 1H), 4.29-4.19 (m, 1H), 3.48 (s, 2H), 3.30 (s, 3H), 3.14-2.98 (m, 1H), 2.99-2.89 (m, 1H), 2.90-2.73 (m, 2H), 2.39 (s, 3H), 2.37-2.30 (m, 1H), 2.28-2.10 (m, 2H), 2.08-1.86 (m, 4H), 1.70-1.51 (m, 1H), 1.38 (s, 6H).

後処理

  1. concentrationThe reaction was concentrated in vacuo
  2. dissolutionthe residue dissolved in the minimum amount of MeOH (˜2 ml)
  3. customThe reaction was quenched by addition of sat. NaHCO3 solution (10 ml) and EtOAc (30 ml)
  4. customThe layers were separated
  5. extractionthe aqueous layer was extracted with EtOAc (2×30 ml)
  6. dry with materialThe combined organic layers were dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customto give the crude product
  10. customThe product was purified by silica flash column chromatography

出典と根拠

ORDレコード
ord-7ac888767cfd4e23b0ca39f5cac3adfc
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09096634B2

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