5-Chloro-6-hydrazinyl-3-nitropyrazin-2-amine → HCID 13255931、化合物

反応式

[Cl:1][C:2]1[N:3]=[C:4]([N+:11]([O-:13])=[O:12])[C:5]([NH2:10])=[N:6][C:7]=1[NH:8][NH2:9].[CH2:14](C(CC)(CC)C([O-])([O-])[O-])[CH3:15]>>[Cl:1][C:2]1[C:7]2[N:6]([C:14]([CH3:15])=[N:9][N:8]=2)[C:5]([NH2:10])=[C:4]([N+:11]([O-:13])=[O:12])[N:3]=1

参加物

反応物 2

HCID 130629835-Chloro-6-hydrazinyl-3-nitropyrazin-2-amine

HCID 21875354Triethylorthoaceate

生成物 1

HCID 13255931HCID 13255931、化合物収率 75%

実験手順

To 5.0 g (0.024 m) 5-chloro-6-hydrazino-3-nitropyrazinamine was added 50 ml of triethylorthoacetate and the resulting suspension was heated at 100° for 2.5 hours. The reaction mixture was cooled, filtered and the resulting dark brown solid washed with chloroform to give 4.1 g (75%) of the titled product as a brown solid, m.p. 220°; H' nmr (DMSO-d6): 9.60 (2H, broad singlet), 3.40 (3H, s); ms:m/e 228.

後処理

temperaturethe resulting suspension was heated at 100° for 2.5 hours
temperatureThe reaction mixture was cooled
filtrationfiltered
washthe resulting dark brown solid washed with chloroform

出典と根拠

ORDレコード: ord-021379e6a0764f1ca27328613ea37c51
出典データセット: uspto-grants-1984_03
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US04438266

反応ノート

読み込み中…

参加物