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Hydrochloric Acid → 2-Amino-4-oxo-3H-indolo[2,3-d]pyrimidine

HRID 1358297
ノート
印刷プレビュー

反応式

HRID 1358297 の反応式
Cl.C([O:4][C:5]([C:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[NH:9][C:8]=1[NH:16][C:17]([NH2:19])=[NH:18])=O)C.[OH-].[Na+].Cl>O>[NH2:18][CH:17]1[N:16]=[C:8]2[N:9]=[C:10]3[C:15]([CH:14]=[CH:13][CH:12]=[CH:11]3)=[C:7]2[C:5](=[O:4])[NH:19]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 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 178469838HCID 178469838、化合物

生成物 1

HCID 700240322-Amino-4-oxo-3H-indolo[2,3-d]pyrimidine収率 80.1%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 2-guanidinoindole-3-carboxylic acid ethyl ester hydrochloride (1.00 g, 3.5 mmol) and sodium hydroxide (1.5 g) in water (50 mL) is heated to gentle reflux for 6 hr followed by the addition of sufficient 5% HCl to adjust the solution to pH 1, and filtration of the resulting mixture through celite, washing the pad with water. The filtrate is extracted with ethyl acetate (3×25 mL), and then basified with solid sodium carbonate. The tan precipitate which slowly forms is collected by filtration, washed with water, and dried in vacuo affording 2-amino-4-oxo-3H-indolo[2,3-d]pyrimidine (561 mg, 78%) as light tan crystals, mp >275 C.

後処理

  1. temperatureis heated
  2. temperatureto gentle reflux for 6 hr
  3. filtrationto pH 1, and filtration of the resulting mixture through celite
  4. washwashing the pad with water
  5. extractionThe filtrate is extracted with ethyl acetate (3×25 mL)
  6. filtrationThe tan precipitate which slowly forms is collected by filtration
  7. washwashed with water
  8. customdried in vacuo

出典と根拠

ORDレコード
ord-c41d47d6f5504ef8a0db7ea91aa6366f
出典データセット
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06596726B1

反応ノート

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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