✦ LIBER ✦

Pyrimidine. III. Study of the Bromination of 5-Acetyl-4-methyl-2-phenylpyrimidine 1

✍ Scribed by Clarke, Ray A.; Graham, Bruce; Christensen, Bert E.

Book ID: 127369169
Publisher: American Chemical Society
Year: 1948
Tongue: English
Weight: 400 KB
Volume: 70
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja01183a064

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Structure of 5-benzoyl-1-methyl-4-phenyl

Structure of 5-benzoyl-1-methyl-4-phenylpyrimidine-2-thione

✍ Özbey, S. ;Kendi, E. ;Akçamur, Y. ;Yıldırım, İ ;. ;Elerman, Y. ;Soylu, H. 📂 Article 📅 1991 🏛 International Union of Crystallography 🌐 English ⚖ 216 KB

5-Acetyl-6-amino-4-methylthio-2-phenylpy

5-Acetyl-6-amino-4-methylthio-2-phenylpyrimidine and its use in the synthesis of functionalized pyrido[2,3-d]pyrimidines and pyrimido-[4,5-d]pyrimidines

✍ A. V. Komkov; A. M. Sakharov; V. S. Bogdanov; V. A. Dorokhov 📂 Article 📅 1995 🏛 Springer 🌐 English ⚖ 442 KB

5-Acetyl-4-methyl-2-pyrimidinylhydrazine

5-Acetyl-4-methyl-2-pyrimidinylhydrazine and 5-(1-hydrazonoethyl)-4-methyl-2-pyrimidinylhydrazine, C7H10N4O and C7H12N6

✍ Cousson, A. ;Nectoux, F. ;Bachet, B. ;Kokel, B. ;Hubert-Habart, M. 📂 Article 📅 1994 🏛 International Union of Crystallography 🌐 English ⚖ 404 KB

ChemInform Abstract: 5-Acetyl-6-amino-4-

ChemInform Abstract: 5-Acetyl-6-amino-4-methylthio-2-phenylpyrimidine and Its Use for Synthesis of Functionalized Pyrido(2,3-d)pyrimidines and Pyrimido(4,5- d)pyrimidines.

✍ A. V. KOMKOV; A. M. SAKHAROV; V. S. BOGDANOV; V. A. DOROKHOV 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

Cyclocondensation of 6-acetyl-4,7-dihydr

Cyclocondensation of 6-acetyl-4,7-dihydro-5-methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine with hydroxylamine and hydrazine

✍ Sergey M. Desenko; Sergey A. Komykhov; Valery D. Orlov; Herbert Meier 📂 Article 📅 1998 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 164 KB

## Abstract The cyclocondensation of 6‐acetyl‐4,7‐dihydro‐5‐methyl‐7‐phenyl[1,2,4]triazolo[1,5‐__a__]pyrimidine (3) with hydroxylamine or hydrazine leads to 3a,4,9,9a‐tetrahydro‐3,9a‐dimethyl‐4‐phenylisoxazolo‐[5,4‐__d__][1,2,4]triazolo[1,5‐__a__]pyrimidine (4a) and 3a,4,9,9a‐tetrahydro‐3,9a‐dimeth

1-[(2-Chlorothiazol-5-yl)methyl]-N′-[

1-[(2-Chlorothiazol-5-yl)methyl]-N′-[2-(2,4-dichlorophenoxy)acetyl]-5-methyl-1H-1,2,3-triazole-4-carbohydrazide

✍ Yan, Man ;Shi, De-Qing 📂 Article 📅 2007 🏛 International Union of Crystallography 🌐 English ⚖ 225 KB

In the title compound, C 16 H 13 Cl 3 N 6 O 3 S, the substituted triazole ring is bound via a methylene bridge to a chlorothiazole unit. There is evidence for significant electron delocalization in the triazolyl system. Both intra-and intermolecular hydrogen bonds are found in the structure.