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Home > Encyclopedia > 2-Amino-4-hydroxy-6-methylpyrimidine

2-Amino-4-hydroxy-6-methylpyrimidine

2-Amino-4-hydroxy-6-methylpyrimidine structure

2-Amino-4-hydroxy-6-methylpyrimidine 

structure
  • CAS No:

    3977-29-5

  • Formula:

    C5H7N3O

  • Chemical Name:

    2-Amino-4-hydroxy-6-methylpyrimidine

  • Synonyms:

    4(3H)-Pyrimidinone,2-amino-6-methyl-;4(1H)-Pyrimidinone,2-amino-6-methyl-;4-Pyrimidinol,2-amino-6-methyl-;2-Amino-6-methyl-4(3H)-pyrimidinone;4-Methylisocytosine;Superacyl;Mecytosine;Superacil;2-Amino-6-hydroxy-4-methylpyrimidine;2-Amino-4-oxo-6-methylpyrimidine;2-Amino-4-hydroxy-6-methylpyrimidine;2-Amino-4-methyl-6-hydroxypyrimidine;2-Amino-6-methyl-4-oxopyrimidine;6-Methylisocytosine;2-Amino-6-methylpyrimidin-4-ol;2-Amino-6-methyl-4-pyrimidinol;2-Amino-6-methyl-4-pyrimidinone;NSC 13145;NSC 23662;NSC 41833;NSC 7893;2-Amino-6-methyl-4(1H)-pyrimidinone;4-Hydroxy-6-methyl-2-pyrimidinamine;2-Amino-6-methylpyrimidin-4(3H)-one;2-Amino-6-methyl-1H-pyrimidin-4-one;2-Amino-6-methyl-1,4-dihydropyrimidin-4-one;2-Amino-6-methyl-3H-pyrimidin-4-one;2-Amino-6-methyl-3,4-dihydropyrimidin-4-one;5414-09-5;175657-83-7

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

white powder


2-amino-6-methylpyrimidin-4(3H)-one is a pyrimidone. It is a tautomer of a 2-amino-4-hydroxy-6-methylpyrimidine.

2-Amino-4-hydroxy-6-methylpyrimidine Basic Attributes

125.13

125.13

3531

223-612-1

K7ZA6H32G8

41833|23662|13145|7893

DTXSID90192847

2933599090

Characteristics

67.5

-0.9

White to cream Powder

1.3±0.1 g/cm3

299-300 °C

253.4ºC at 760 mmHg

187.2±25.7 °C

1.638

Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Safety Information

IRRITANT

NONH for all modes of transport

3

36/37/38

24/25-36/37/39-26-22

UW7362250

Xi

Stable under normal temperatures and pressures.

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 6 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

2-amino-6-methylpyrimidin-4-one

2-Amino-4-hydroxy-6-methylpyrimidine Use and Manufacturing

Methods of Manufacturing

The above compound was prepared using a previously reportedmethod with minor modifications [26] as shown in Scheme 1. To asolution of guanidine (2.02 g, 33.84 mM) in acetone/ethanol mixture(1:2), a solution of acetoacetic ester (4.40 g, 33.86 mM) in acetone/ethanol was added dropwise and the resulting solution wasstirred at room temperature for 10 h. The solid product obtainedwas separated by filtration and recrystallized from acetic acid toobtain colorless crystals.Yield: 1.36 g (52percent). 1H NMR (400 MHz, CDCl3, ppm), d: 11.09 (s, 1H, OH), 5.92 (s, 2H, NH2), 5.14 (s, 1H, Ar–H), 2.14 (s, 3H, Ar–CH3).13C NMR (100 MHz, CDCl3, ppm) d: 162.3, 161.1, 155.3, 102.5, 23.9.ESI-MS calc. for C5H7N3O [M+]: 125.06; found 126.07 [M++1].Added to the mixture obtained in step a)Amount of anhydrous methanol dissolved, Into guanidine hydrochloride 95.5g (1mol)Heated to 100 reflux 3h, The mixture of solvents evaporated to dryness, Add the right amount of distilled water to just dissolve, Let cool to room temperature, With 1mol / L dilute hydrochloric acid to adjust the PH value to 6.5, A solid precipitation, suction filtration, Rinse with deionized water, The resulting wet finished product is at a temperature of 60 ° CVacuum drying oven available 12h availableAbout 77.7 g of 2-amino-4-hydroxy-6-methylpyrimidine.The product is 2-amino-4-hydroxy-6-methylpyrimidine, Purity of 99percentYield 62.1percentTo a solution of compound 3 (0.16gm, 0.0013 mol) in toluene, phosphorous oxychloride (0.9 ml, 0.0104 mol) [15] was added and heated at 110 C for 30 min. The excess POCl3 was distilled offand gummy residue was poured in to ice cold water. Neutralizationwith NaHCO3 gave yellow solid which was recrystallized frommethanol.Diisopropyl 2-chloroethoxymethylphosphonate (15 mL, 62.5 mmol) was added to a mixture of

Uses

Anconite intermediate.

Computed Properties

Molecular Weight:125.13
XLogP3:-0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Exact Mass:125.058911855
Monoisotopic Mass:125.058911855
Topological Polar Surface Area:67.5
Heavy Atom Count:9
Complexity:204
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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