tert-Butyl methyl ether → Pyrazine-2-carboxamidine hydrochloride

HRID 1295681

反応式

HRID 1295681 の反応式
C[O-].[Na+].[C:4]([C:6]1[CH:11]=[N:10][CH:9]=[CH:8][N:7]=1)#[N:5].[Cl-:12].[NH4+:13].C(OC)(C)(C)C>CO>[ClH:12].[N:7]1[CH:8]=[CH:9][N:10]=[CH:11][C:6]=1[C:4]([NH2:13])=[NH:5]

参加物

6

反応物 4

HCID 15413tert-Butyl methyl etherHCID 25517Ammonium ChlorideHCID 73172PyrazinecarbonitrileHCID 10942334Sodium Methoxide

生成物 1

HCID 470895Pyrazine-2-carboxamidine hydrochloride収率 95%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
30 °C

実験手順

To a solution of sodium methoxide (NaOCH3) (51.4 g, 0.952 mol) in methanol (3800 ml) there is added cyanopyrazine (1.00 KG, 9.53 mol) slowly at room temperature. The mixture is heated to 30° C. and stirred for 6 h. The mixture is cooled to 25° C. followed by the addition of ammonium chloride (NH4Cl) (572 g, 10.5 mol). The reaction mixture is stirred for 22 h and methyl t-butyl ether (4000 mL) is added and the mixture is stirred for 15 min forming a solid. The solid is filtered and washed with methyl t-butyl ether (2×1000 mL) then dried at 40° C./0–10 mmHg for 17 h to give white solid product (1435 g) in 95% yield with 95% HPLC purity. 1H NMR (DMSO-D6): δ 9.7 (bs, 3H), 9.49 (d, 1H, J=1.5 Hz), 9.04 (m, 1H), 8.93 (t, 1H, J=1.5 Hz)

後処理

  1. temperatureThe mixture is cooled to 25° C.
  2. stirringThe reaction mixture is stirred for 22 h
  3. stirringthe mixture is stirred for 15 min
  4. customforming a solid
  5. filtrationThe solid is filtered
  6. washwashed with methyl t-butyl ether (2×1000 mL)
  7. customthen dried at 40° C./0–10 mmHg for 17 h

出典と根拠

ORDレコード
ord-d984898d78384b6285459b750d9e38a7
出典データセット
uspto-grants-2007_07
特許番号
US07244736B2

関連ノート

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