2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE

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Products Intro: Product Name:5,6,7,8-Tetrahydro-1,6-naphthyridine
CAS:80957-68-2
Purity:98% (Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:80957-68-2
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Products Intro: Product Name:5,6,7,8-Tetrahydro-1,6-naphthyridine
CAS:80957-68-2
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Products Intro: Product Name:5,6,7,8-Tetrahydro-1,6-naphthyridine
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Products Intro: Product Name:5,6,7,8-Tetrahydro-1,6-naphthyridine
CAS:80957-68-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-04466

2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE manufacturers

2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE Basic information
Product Name:2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE
Synonyms:5,6,7,8-TETRAHYDRO-[1,6]NAPHTHYRIDINE;1,6-Naphthyridine, 5,6,7,8-tetrahydro-;5,6,7,8-tetrahydro-1,6-naphthyridine(SALTDATA: 2HCl 0.5H2O);5,6,7,8-tetrahydro-1,6-naphthyridine HCl Salt;5,6,7,8-Tetrahydro-1,6phthyridine;5,6,7,8-tetrahydropyrido[4,3-b]pyridine
CAS:80957-68-2
MF:C8H10N2
MW:134.18
EINECS:
Product Categories:Heterocycle-Pyridine series;CHIRAL CHEMICALS
Mol File:80957-68-2.mol
2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE Structure
2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE Chemical Properties
Boiling point 247.6±30.0 °C(Predicted)
density 1.068±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka7.95±0.20(Predicted)
Safety Information
MSDS Information
2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE Usage And Synthesis
Uses5,6,7,8-Tetrahydro-1,6-naphthyridine is used in the synthetic preparation of quinolizidinone carboxylic acid selective M1 allosteric modulators.
Synthesis
6-benzyl-7,8-dihydro-5H-1,6-naphthyridine

75510-02-0

2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE

80957-68-2

6-Benzyl-5,6,7,8-tetrahydro-1,6-naphthyridine (3.9 g, 17.4 mmol) was used as a starting material and dissolved in 60 mL of acetic acid. A 0.4 g palladium/carbon catalyst was added. The reaction solution was transferred to a hydrogen reaction vessel and after three displacements with hydrogen, the reaction was carried out at 50 °C for 48 hours. After completion of the reaction, the catalyst was removed by filtration. The solvent was removed by distillation under reduced pressure and the resulting crude product was purified by column chromatography using a solvent mixture of dichloromethane and methanol (5:1, v/v) to afford the target product 5,6,7,8-tetrahydro-1,6-naphthyridine (1.48 g, 64% yield).

References[1] Chemical and Pharmaceutical Bulletin, 1984, vol. 32, # 7, p. 2522 - 2529
[2] Patent: CN108250128, 2018, A. Location in patent: Paragraph 0638; 0640; 0643; 0644
[3] Patent: WO2009/56556, 2009, A1. Location in patent: Page/Page column 41
[4] Journal of Medicinal Chemistry, 2004, vol. 47, # 21, p. 5167 - 5182
2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE Preparation Products And Raw materials
Raw materials3-BROMO-5,6,7,8-TETRAHYDRO-1,6-NAPHTHYRIDINE-->6-benzyl-7,8-dihydro-5H-1,6-naphthyridine
Tag:2-P-TOLYL-4,5,6,7-TETRAHYDRO-OXAZOLO[5,4-C]PYRIDINE(80957-68-2) Related Product Information
2-Chloro-6-(trifluoromethyl)nicotinonitrile 1,6-Naphthyridine, 2-chloro-5,6,7,8-tetrahydro- 5-chloro-1,2,3,4-tetrahydro-1,6-naphthyridine 5,6,7,8-TETRAHYDRO-1,6-NAPHTHYRIDIN-3-OL 6-benzyl-5,6,7,8-tetrahydro-1,6-naphthyridin-2(1H)-one 5,6,7,8-TETRAHYDRO-6-(PHEHYLMETHYL)-1,6-NAPHTHYRIDIN-3-AMINE 5-Bromo-1,2,3,4-tetrahydro-[1,7]naphthyridine METHYL 6-BROMO-2-OXO-1,2,3,4-TETRAHYDRO-1,8-NAPHTHYRIDINE-3-CARBOXYLATE 3-BROMO-5,6,7,8-TETRAHYDRO-1,6-NAPHTHYRIDINE 5,6,7,8-tetrahydro-2,6-naphthyridin-1-amine 3-methyl-5,6,7,8-tetrahydro-1,6-naphthyridine 5,6,7,8-tetrahydro-2,6-naphthyridin-1(2H)-one hydrochloride Pyrido[2,3-b][1,6]naphthyridine, 6,7,8,9-tetrahydro- (9CI) 4-(3,4-DIHYDROPYRIDO[4,3-B]-1,6-NAPHTHYRIDIN-2(1H)-YL)-4-OXOBUTANOICACID 1,2,3,4-TETRAHYDROPYRIDO[4,3-B]-[1,6]-NAPHTHYRIDINE AKOS USSH-4110802 2-BENZYL-1,2,3,4-TETRAHYDROPYRIDO[4,3-B][1,6]NAPHTHYRIDINE Pyrido[2,3-b][1,6]naphthyridine, 7-acetyl-6,7,8,9-tetrahydro- (9CI)

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