HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[(Thiazol-2-yl)methylthio]ethylamine → 2-[2-(2-Thiazolylmethylthio)ethylamino]-5-(3-methoxybenzyl)-4-pyrimidone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[(Thiazol-2-yl)methylthio]ethylamine | HCID 12923403 | — |
| Reactant | 2-Nitroamino-5-(3-methoxybenzyl)-4-pyrimidone | HCID 20279274 | — |
| Product | 2-[2-(2-Thiazolylmethylthio)ethylamino]-5-(3-methoxybenzyl)-4-pyrimidone | HCID 12951556 | 41.9% |
Reaction Steps
2-(2-Thiazolylmethylthio)ethylamine (2.00 g) and 2-nitroamino-5-(3-methoxybenzyl)-4-pyrimidone (1.58 g) were fused together at 130° for 4 hours. The mixture was triturated with hot water and the residue was recrystallised from 2-propanol to give 2-[2-(2-thiazolylmethylthio)ethylamino]-5-(3-methoxybenzyl)-4-pyrimidone (0.93 g), m.p. 122°-4°. A sample was treated with hydrogen chloride in ethanol and after recrystallision from isopropanol/methanol it had m.p. 104°-6° and gave analytical data corresponding to a hemihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04227000 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-90b144ecc7984649ad945ae98998f377 |
| Source note | uspto-grants-1980_10 |