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2-amino-4,5-dimethyl

Imidazole, 2-amino-4,5-dimethyl-pK, 5, 384 B-76M140701, 70AHC(12)103, 80AHC(27)241>... [Pg.27]

Thiazoline, trans-2-amino-4,5-dimethyl-synthesis, 6, 310 2-Thiazoline, 2-aryl-synthesis, 6, 307, 308, 309 2-Thiazoline, 2-arylamino-tautomerism, 6, 248 2-Thiazoline, 2-dialkylamino-synthesis, 6, 308 2-liiiazoline, 5-imino-synthesis, 5, 461 2-"niiazoline, 2-mercapto-hydrolysis, 6, 272 oxidation, 6, 272 synthesis, 6, 307 2-Thiazoline, 2-methyl-aldehyde synthesis from, 1, 469 2-Thiazoline, 2-methyl-acetylation, 6, 270 acylation, 6, 270 H NMR, 6, 243... [Pg.875]

Thiophene-3-carboxylic acid, 2-amino-4,5-dimethyl-protonation, 4, 811... [Pg.893]

Athoxymethylenamino-4,5-dimethyl-3-cyan-thiophen Eine Aufschlammung von 7,61 g (0,05 Mol) 2-Amino-4,5-dimethyl-3-cyan-thiophen in 40 ml Orthoameisensaure-triathylester wird unter Riih-ren 5 Stdn. am RiickfluB erhitzt. Man engt ein und saugt den kristallinen Ruckstand mit Petrolather ab Ausbeu-te 9,15-10,2 g (88-98% d.Th.) F 58,5-59,5°. [Pg.351]

Figure 6 Structure of PD81,723, (2-amino-4,5-dimethyl-trienyl)[3-(trifluoro-methyl) phenyl]methanone and adenosine At agonists/antagonists. Figure 6 Structure of PD81,723, (2-amino-4,5-dimethyl-trienyl)[3-(trifluoro-methyl) phenyl]methanone and adenosine At agonists/antagonists.
PD81,723 (2-Amino-4,5-dimethyl-3-thienyl)-[3(trifluoromethyl) phenyl]methanone... [Pg.244]

Phenyl-5-pyrazolo)-benzimidazole allgemeine Arbeitsvorschrift206 Einc Mischung von 1,0 g (4,0 mmol) 5-(2-Amino-anilino)-3-phenyl-pyrazol (R1 = H) bzw. 1,0 g (3,6 mmol) 5-(2-Amino-4,5-dimethyl-anilino)-3-phenyl-pyrazol (R1 = CH3) werden mit 5 ml Orthocarbonsaure-triethylester in Xylol 2 h am RiickfluB erhitzt. Nach dem Abziehen des Losungsmittels i. Vak, crhalt man ein Ol, das bei Zugabe von kaltem Diethylether kristallisiert. Die Produkte werden durch Umkristallisieren aus Ethanol gercinigt. [Pg.263]

Aziridines also undergo ring enlargement on treatment with thiocyanic acid cis- and trans-2,3-dimethylaziridines (223) thus gave trans- and cw-2-amino-4,5-dimethyl-2-thiazolines (224) stereospecifically (72JOC4401). [Pg.574]

N- Unsubstituted aziridines react with thiocyanic acid with ring enlargement, producing 2-amino-Az-thiazolines. The reaction proceeds stereospecifically with 100% Walden inversion as illustrated in Scheme 229. c -2,3-Dimethylaziridine (369) gives exclusively trans-2-amino-4,5-dimethyl-Az-thiazoline (371) (72JOC4401). [Pg.310]

Aziridines also undergo ring enlargement when treatment with thiocyanic acid, cis- and tran5-2,3-Dimethylaziridine (470) with thiocyanic acid gave exclusively trans- and cis-2-amino-4,5-dimethyl-2-thiazoline (471) (72JOC4401). [Pg.156]

Amino-3,4-dimethyl- 53 2-Amino-4,5-dimethyl- 16, 63, 94, 109, 158 2-Ami n o-5-(l -dimethylamino-ethyl)-195 2-Amino-5-(2-dimethylamino-ethyl)- 195 4-Amino-2-dimethylamino-5-phenyl- 101 2-Amino-4,5-diphenyl- 16, 101... [Pg.1135]

Amino-3,4-dimcthyl-5-(5-nitro-2-furyl)- 209 2-Amino-4,5-dimethyl-3-phenyl- -chlorid 159... [Pg.1152]

N)-Amino]-3,5-dimethyl- 599 [l-15N]-l-Amino-3,5-dimethyl- 711 5-Amino-l,3-dimethyl- 586 5(3)-(2-Amino-4,5-dimethyl-anilino)-3(5)-phenyl-566... [Pg.1159]

Oxo-3-methyl-2-anilinomethylen-tetrahydro- 253 5- Oxo- 3-phenyl- 4- [a - (2- amino- anilino)-benzyliden]-4,5-dihydro- 481 5-Oxo-3-phenyl-4-[2-(2-amino-4,5-dimethyl-anilino) -benzyliden]- 4,5- dihy dro- 481 5- Oxo- 3-phenyl- 4- [ a -(2-amino- 4-m ethyl-anilino)-benzyliden]-4,5-dihydro- 481 5-Oxo-3-phenyl-4-(oc-hydroxy-benzyliden)-4,5-dihydro- 548... [Pg.843]

See other pages where 2-amino-4,5-dimethyl is mentioned: [Pg.875]    [Pg.928]    [Pg.929]    [Pg.235]    [Pg.148]    [Pg.242]    [Pg.875]    [Pg.213]    [Pg.214]    [Pg.221]    [Pg.312]    [Pg.888]    [Pg.875]    [Pg.3339]    [Pg.16]    [Pg.63]    [Pg.94]    [Pg.158]    [Pg.159]    [Pg.566]    [Pg.1152]    [Pg.1186]    [Pg.845]   
See also in sourсe #XX -- [ Pg.148 ]



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1 -Amino-2,3-dimethyl-2-pentanol

1- Amino-3- -6,6-dimethyl-5,6,7,8-tetrahydro

1-Amino-2-brom-3,3-dimethyl

1-Amino-2.3-dimethyl-4-phenyl- -iodid

1.8- Naphthyridine, 2-amino-5,7-dimethyl

2-Amino-3,5-dimethyl- -bromid

3- Amino-1,4-dimethyl-5//-pyrido

3- Amino-1,4-dimethyl-5//-pyrido indole

3- Amino-6-chlor-4,5-dimethyl

3-Amino-1,4-dimethyl-5H-pyrido

3-Amino-2,3-dimethyl-2-butano

3-Amino-6,7-dimethyl-2-quinoxalinecarbonitrile

3.5- Dimethyl-4-amino- 1,2,4-triazole

4-Amino-2,3-dimethyl-8-hydroxy- -Hydrochlorid

4-amino-1,3-dimethyl-benzene

5- Amino-3,4-dimethyl-1,2-oxazole

5- Amino-4,5-dimethyl-4-hydroxy

6- Amino-1,3-dimethyl-5-nitrosouracil

6- amino-l,3dimethyluracil reaction with dimethyl acetylene

6-Amino-2,4-dimethyl pyrimidine

DiMethyl amino benzaldehyde and

Dimethyl amino pyridine

Dimethyl-4-amino aniline

Dimethyl-amino-cinnamaldehyde

Glutarates dimethyl 3-amino

Isoxazole, 4-amino-3,5-dimethyl

Propionic acid, 3-amino-2,2-dimethyl-3-phenylsynthesis

Purine 6-amino-2,8-dimethyl

Pyrazole, 1-amino-3,5-dimethyl-, reaction

Synthesis of 4-Amino-3,5-dimethyl-l,2,4-triazole

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