Hydrochloric Acid → N6-(3-Iodobenzyl)-2-chloro-5'-O-cyclopropyladenosine

HRID 6674

反応式

HRID 6674 の反応式
[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[C@@H:11]2[O:23][C@H:22]([CH2:24][O:25][CH:26]3[CH2:28][CH2:27]3)[C@@H:17]([O:18]C(=O)C)[C@H:12]2[O:13]C(=O)C)=[C:4](Cl)[N:3]=1.[I:30][C:31]1[CH:32]=[C:33]([CH:36]=[CH:37][CH:38]=1)[CH2:34][NH2:35].Cl>>[I:30][C:31]1[CH:32]=[C:33]([CH:36]=[CH:37][CH:38]=1)[CH2:34][NH:35][C:4]1[C:5]2[N:6]=[CH:7][N:8]([C:9]=2[N:10]=[C:2]([Cl:1])[N:3]=1)[C@@H:11]1[O:23][C@H:22]([CH2:24][O:25][CH:26]2[CH2:28][CH2:27]2)[C@@H:17]([OH:18])[C@H:12]1[OH:13]

参加物

4

反応物 3

HCID 313Hydrochloric AcidHCID 970123-IodobenzylamineHCID 111130652,6-dichloro-9-(2,3-di-O-acetyl-5-O-cyclopropyl-beta-D-ribofuranosyl)-purine

生成物 1

HCID 10896988N6-(3-Iodobenzyl)-2-chloro-5'-O-cyclopropyladenosine

実験手順

Method B. The reaction was carried out with 2,6-dichloro-9-(2,3-di-O-acetyl-5-O-cyclopropyl-β-D-ribofuranosyl)-purine (65, 483 mg, 1.08 mmol) and 3-iodobenzylamine.HCl (1.63 mmol, 439 mg). The mixture was purified by column chromatography (eluens 5% MeOH in CH2Cl2). Yield 435 mg (0.78 mmol, 72%), mp 94–96° C.; Rf 0.49 (10% MeOH in CH2Cl2); 1H NMR (DMSO-d6) δ 8.93 (t, 1H, J=6.18 Hz, NH), 8.33 (s, 1H, H-8), 7.73 (s, 1H, CCHCI), 7.59 (d, 1H, J=7.90 Hz, CCHCHCH), 7.34 (d, 1H, J=7.55 Hz, CCHCH), 7.11 (t, 1H, J=7.55 Hz, CCHCH), 5.82 (d, 1H, J=5.14 Hz, H-1′), 5.54 (d, 1H, J=5.84 Hz, OH-2′), 5.30 (d, 1H, J=5.15 Hz, OH-3′), 4.61–4.48 (m, 3H, H-2′, NHCH2), 4.09–3.98 (m, 2H, H-3′,4′), 3.68–3.58 (m, 2H, H-5′), 0.45–0.41 (m, 4H, cyclopropyl); MS m/z 559 (M+H)+; Anal. (C20H21ClIN5O4.0.5 H2O) C, H, N.

後処理

  1. customThe mixture was purified by column chromatography (eluens 5% MeOH in CH2Cl2)

出典と根拠

ORDレコード
ord-6fb65ac27b4e4300a6d9d193585491c1
出典データセット
uspto-grants-2006_08
特許番号
US07084127B2

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