tert-Butylhydrazine monohydrochloride → 1-tert-Butyl-5-(4-nitrophenyl)-1H-pyrazole

反応式

[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:14](B3OC(C)(C)C(C)(C)O3)=[CH:13][N:12](CC(OC(C)(C)C)=O)[N:11]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2].Cl.[C:33](NN)([CH3:36])([CH3:35])[CH3:34]>>[CH3:34][C:33]([N:11]1[C:10]([C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=2)=[CH:14][CH:13]=[N:12]1)([CH3:36])[CH3:35]

参加物

反応物 2

HCID 81889tert-Butylhydrazine monohydrochloride

HCID 866173901,1-dimethylethyl [3-(4-nitrophenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]acetate

生成物 1

HCID 534855271-tert-Butyl-5-(4-nitrophenyl)-1H-pyrazole

実験手順

Following the procedure described for Intermediate 1 with t-butylhydrazine hydrochloride, provided the title compound as the major isomer (80%). ESMS (M-C(CH3)3+2H): 190.0; HNMR (400 MHz, d6-DMSO) δ 8.32 (d, 2H), 7.7 (d, 2H), 7.48 (d, 1H), 6.25 (d, 1H), 1.42 (s, 9H)

出典と根拠

ORDレコード: ord-532c554ed4fb44c495bb1d0cc3f79b9c
出典データセット: uspto-grants-2009_02
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US07495102B2

反応ノート

読み込み中…

参加物