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Sodium Nitrite → 3-beta-D-Ribofuranosylthiazolo[4,5-d]pyrimidine-2,5,7(4H,6H)-trione

HRID 2248931
ノート
印刷プレビュー

反応式

HRID 2248931 の反応式
N[C:2]1[NH:3][C:4](=[O:21])[C:5]2[S:10][C:9](=[O:11])[N:8]([C@@H:12]3[O:18][C@H:17]([CH2:19][OH:20])[C@@H:15]([OH:16])[C@H:13]3[OH:14])[C:6]=2[N:7]=1.N([O-])=[O:23].[Na+]>C(O)(=O)C.O>[C@@H:12]1([N:8]2[C:6]3[NH:7][C:2](=[O:23])[NH:3][C:4](=[O:21])[C:5]=3[S:10][C:9]2=[O:11])[O:18][C@H:17]([CH2:19][OH:20])[C@@H:15]([OH:16])[C@H:13]1[OH:14]
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 23668193Sodium NitriteHCID 135409474Isatoribine Anhydrous

生成物 1

HCID 145057353-beta-D-Ribofuranosylthiazolo[4,5-d]pyrimidine-2,5,7(4H,6H)-trione

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 962Water溶媒

実験手順

To a suspension of 7 (0.76 g, 2.4 mmol) in glacial acetic acid (150 mL) was added dropwise a solution of sodium nitrite (1.5 g, 21.7 mmol) in water (15 mL) with stirring. After 30 min the suspension became clear and stirring was continued at room temperature overnight. The white solid which had separated was filtered, washed with cold water and dried. Recrystallization from hot water gave fine colorless crystals of 8: yield 0.3 g, 40%: mp 250° C. dec.: UV λmax (pH 1) 293 nm (ε 5500): UV λmax (pH 7) 212 nm (ε 14,200), 301 (6100): UV λmax (pH 11) 204 nm (ε 21,900), 301 (5600). Anal Calcd. for C10H11N3O7S: C, 37.86: H, 3.49: N, 13.24: S, 10.10. Found: C, 37.81: H, 3.42: N, 13.01: S, 10.01.

後処理

  1. stirringstirring
  2. waitwas continued at room temperature overnight
  3. customThe white solid which had separated
  4. filtrationwas filtered
  5. washwashed with cold water
  6. customdried
  7. customRecrystallization from hot water
  8. customgave fine colorless crystals of 8

出典と根拠

ORDレコード
ord-b280bd1b54a94b3fa77843820e398502
出典データセット
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05041426

反応ノート

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