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4-[3-(2,4-Diamino-6-oxo-1,6-dihydro-pyrimidin-5-yl)-4,4-dimethoxy-butyl]-benzoic acid tert-butyl ester

Base Information Edit
  • Chemical Name:4-[3-(2,4-Diamino-6-oxo-1,6-dihydro-pyrimidin-5-yl)-4,4-dimethoxy-butyl]-benzoic acid tert-butyl ester
  • CAS No.:146943-41-1
  • Molecular Formula:C21H30N4O5
  • Molecular Weight:418.493
  • Hs Code.:
  • Mol file:146943-41-1.mol
4-[3-(2,4-Diamino-6-oxo-1,6-dihydro-pyrimidin-5-yl)-4,4-dimethoxy-butyl]-benzoic acid tert-butyl ester

Synonyms:4-[3-(2,4-Diamino-6-oxo-1,6-dihydro-pyrimidin-5-yl)-4,4-dimethoxy-butyl]-benzoic acid tert-butyl ester

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Chemical Property of 4-[3-(2,4-Diamino-6-oxo-1,6-dihydro-pyrimidin-5-yl)-4,4-dimethoxy-butyl]-benzoic acid tert-butyl ester Edit
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Technology Process of 4-[3-(2,4-Diamino-6-oxo-1,6-dihydro-pyrimidin-5-yl)-4,4-dimethoxy-butyl]-benzoic acid tert-butyl ester

There total 7 articles about 4-[3-(2,4-Diamino-6-oxo-1,6-dihydro-pyrimidin-5-yl)-4,4-dimethoxy-butyl]-benzoic acid tert-butyl ester 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:
Guidance literature:
Multi-step reaction with 7 steps
1: 94 percent / toluene / 1 h / Heating
2: 100 percent / H2 / 10percent Pd/C / ethyl acetate; methanol / 4 h
3: 99 percent / LiBH4 / diethyl ether / 15 h / Ambient temperature
4: 87 percent / oxalyl chloride, DMSO / CH2Cl2 / 0.25 h / -60 °C
5: 1) t-BuOK / 1) THF, toluene, 10 min, 2) toluene, 0 deg C, 20 min
6: 1) CH2Cl2, molecular sieves 3A, UV, 0 - 5 deg C
7: 74 percent / 1 M BuOK / tetrahydrofuran; 2-methyl-propan-2-ol / Heating
With lithium borohydride; oxalyl dichloride; potassium tert-butylate; hydrogen; potassium n-butoxide; dimethyl sulfoxide; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; ethyl acetate; toluene; tert-butyl alcohol;
DOI:10.1021/jo00059a016
Guidance literature:
Multi-step reaction with 6 steps
1: 100 percent / H2 / 10percent Pd/C / ethyl acetate; methanol / 4 h
2: 99 percent / LiBH4 / diethyl ether / 15 h / Ambient temperature
3: 87 percent / oxalyl chloride, DMSO / CH2Cl2 / 0.25 h / -60 °C
4: 1) t-BuOK / 1) THF, toluene, 10 min, 2) toluene, 0 deg C, 20 min
5: 1) CH2Cl2, molecular sieves 3A, UV, 0 - 5 deg C
6: 74 percent / 1 M BuOK / tetrahydrofuran; 2-methyl-propan-2-ol / Heating
With lithium borohydride; oxalyl dichloride; potassium tert-butylate; hydrogen; potassium n-butoxide; dimethyl sulfoxide; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; ethyl acetate; tert-butyl alcohol;
DOI:10.1021/jo00059a016
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