3-Benzyloxymethyl-6-methoxy-3,4-dihydro-pyrimido[1,6-c][1,3]oxazin-8-one

Base Information

Chemical Name:3-Benzyloxymethyl-6-methoxy-3,4-dihydro-pyrimido[1,6-c][1,3]oxazin-8-one
CAS No.:187093-94-3
Molecular Formula:C₁₆H₁₈N₂O₄
Molecular Weight:302.33
Hs Code.:

Synonyms:3-Benzyloxymethyl-6-methoxy-3,4-dihydro-pyrimido[1,6-c][1,3]oxazin-8-one

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Chemical Property of 3-Benzyloxymethyl-6-methoxy-3,4-dihydro-pyrimido[1,6-c][1,3]oxazin-8-one

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Technology Process of 3-Benzyloxymethyl-6-methoxy-3,4-dihydro-pyrimido[1,6-c][1,3]oxazin-8-one

There total 5 articles about 3-Benzyloxymethyl-6-methoxy-3,4-dihydro-pyrimido[1,6-c][1,3]oxazin-8-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 23.0%

: 187093-93-2
4-(3-Benzyloxy-2-methylsulfanylmethoxy-propyl)-2,6-dimethoxy-pyrimidine

: 187093-94-3
3-Benzyloxymethyl-6-methoxy-3,4-dihydro-pyrimido[1,6-c][1,3]oxazin-8-one

Guidance literature:: With iodine; In tetrahydrofuran; for 72h; Ambient temperature;
DOI:10.3987/COM-96-7607

Reference yield:

: 60656-87-3
benzyloxyacetoaldehyde

: 187093-94-3
3-Benzyloxymethyl-6-methoxy-3,4-dihydro-pyrimido[1,6-c][1,3]oxazin-8-one

Guidance literature:: Multi-step reaction with 3 steps

1: 58 percent / n-BuLi / tetrahydrofuran / -70 deg C then -55 deg C, 3 h

2: 44 percent / Ac₂O / 36 h / Ambient temperature

3: 23 percent / I₂ / tetrahydrofuran / 72 h / Ambient temperature

With n-butyllithium; iodine; acetic anhydride; In tetrahydrofuran;
DOI:10.3987/COM-96-7607

Reference yield:

: 42783-78-8
benzyloxyacetaldehyde diethyl acetal

: 187093-94-3
3-Benzyloxymethyl-6-methoxy-3,4-dihydro-pyrimido[1,6-c][1,3]oxazin-8-one

Guidance literature:: Multi-step reaction with 4 steps

1: 44 percent / TFA, water / CHCl₃ / 1 h / Ambient temperature

2: 58 percent / n-BuLi / tetrahydrofuran / -70 deg C then -55 deg C, 3 h

3: 44 percent / Ac₂O / 36 h / Ambient temperature

4: 23 percent / I₂ / tetrahydrofuran / 72 h / Ambient temperature

With n-butyllithium; water; iodine; acetic anhydride; trifluoroacetic acid; In tetrahydrofuran; chloroform;
DOI:10.3987/COM-96-7607