反応 #1483049

ord-92064e337d62481ba3bdbac56edfb73e

反応方程式

O=N[O-].[Na+]
sodium nitrite
CCOC(=N)c1ccc(CO)cc1.Cl
4-(hydroxymethyl)-benzenecarboximidic acid, ethyl ester, hydrochloride
CC(=O)O.N=CN
formamidine acetate
NN
hydrazine
OCc1ccc(-c2nncnn2)cc1
(4-(1,2,4,5-tetrazin-3-yl)phenyl)methanol
収率 21.3%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGto stir for 15 minutes
  2. 2
    その他The aqueous crude reaction
  3. 3
    抽出was subsequently extracted with methylene chloride (4×10 mL)
  4. 4
    乾燥The organic extracts were dried with MgSO4
  5. 5
    その他After solvent removal
  6. 6
    その他the crude pink product was purified by flash chromatography (silica gel)
  7. 7
    洗浄first washing with 100% methylene chloride

実験手順

To a mixture of 4-(hydroxymethyl)-benzenecarboximidic acid, ethyl ester, hydrochloride (1 mmol, 216 mg) and formamidine acetate (5 mmol, 521 mg) was added anhydrous hydrazine (20 mmol, 630 uL) the resulting viscous oil was allowed to stir. After 1 hour, acetic acid (3 mL) was added followed by sodium nitrite (690 mg, 10 mmol) as a finely divided powder. The now bright pink solution was allowed to stir for 15 minutes and then diluted with 15 mL of water. The aqueous crude reaction was subsequently extracted with methylene chloride (4×10 mL). The organic extracts were dried with MgSO4. After solvent removal, the crude pink product was purified by flash chromatography (silica gel) first washing with 100% methylene chloride, followed by methylene chloride with 1% methanol, giving (4-(1,2,4,5-tetrazin-3-yl)phenyl)methanol (40 mg, 21%) as a bright pink solid. LRMS-ESI [M+H]− calcd. for C9H9N4O−: 189.08, found: 188.8.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08900549B2uspto-grants-2014_12