Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Sadao Nishigaki"'
Autor:
Katsurada Masanori, Toshimasa Ishida, Masatoshi Sakae, Fumio Yoneda, Mayumi Watanabe, Sadao Nishigaki
Publikováno v:
Journal of Heterocyclic Chemistry. 34:157-160
The reaction of 2-bromoethylamine 1 with methylisothiocyanate 2 under mild condition gave 2-methyl-amino-2-thiazoline 3 as the major product together with two kinds of byproducts, 3-(N-methylthiocar-bamoyl)-2-methyliminothiazolidine 4 and N,N′-dime
Publikováno v:
Japanese Journal of Hospital Pharmacy. 5:118-122
Publikováno v:
The Journal of Organic Chemistry. 44:3830-3834
Autor:
Masatsugu Higuchi, Hashime Kanazawa, Misuzu Ichiba, Fumio Yoneda, Keitaro Senga, Sadao Nishigaki
Publikováno v:
Journal of Heterocyclic Chemistry. 15:641-644
A novel synthesis of 8-arylaminotheophyllines (8a-e) by the reaction of 5-arylazo-6-ethoxy-methyleneamino-1,3-dimethyluracils (2a-e) or 5-arylazo-1,3-dimethyl-6-dimethylaminomethylene-aminouracils (3a-e) with sodium dithionite in formic acid is descr
Publikováno v:
Journal of Heterocyclic Chemistry. 15:359-363
Treatment of 1,3-dimethyl-6-hydrazinouracil with the appropriate dimethylformamide dialkylacetal afforded the, corresponding 2-alkyl-5,7-dimethylpyrazolo[3,4-d]pyrimidine-4,6-(5H,7H)diones. The reaction of 1,3-dimethyl-6-(α-methylbenzylidenehydrazin
Publikováno v:
Chemical and Pharmaceutical Bulletin. 26:367-373
A new synthesis of 1, 3-dimethyl-6-azalumazines (isofervenulins) is described. The reaction of 6-amino-1, 3-dimethyl-5-nitrosouracil (I) with acid hydrazides in refluxing aprotic solvents such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO) or
Publikováno v:
Journal of Heterocyclic Chemistry. 19:769-773
Reaction of 5-arylazo-6-arylidenehydrazino-1,3-dimethyluracils (II), prepared by the treatment of 6-aryl-idenehydrazino-1,3-dimethyluracils (I) with diazotized arylamines, with dimethylformamide dimethylacetal resulted in the formation of pyrimido[5,
Publikováno v:
The Journal of Organic Chemistry. 43:1677-1683
Autor:
Sadao Nishigaki, Nobuyuki Shimizu, Yoshinobu Nakai, Keiji Yamamoto, Katsuhide Terada, Takeshi Uchida
Publikováno v:
Chemical and Pharmaceutical Bulletin. 30:2629-2632
The crystal structure of ftorafur, C8H9FN2O3, has been determined by single-crystal X-ray diffraction techniques. The crystal is triclinic, space group P1 ; its unit-cell dimensions are a=8.994 (8), b=16.612 (9), c=5.981 (5) A, α=86.40 (6), β=94.06
Publikováno v:
Japanese Journal of Hospital Pharmacy. 4:142-146