HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phthalimidoethanethiol → 4-Amino-2-[(2-phthalimidoethyl)thiomethyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phthalimidoethanethiol | HCID 96248 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-(Chloromethyl)pyrimidin-4-amine | HCID 21298827 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Amino-2-[(2-phthalimidoethyl)thiomethyl)pyrimidine | HCID 21298818 | — |
Reaction Steps
A solution of 4-amino-2-chloromethylpyrimidine (11.6 g.) in methanol (20 ml.) was added over 15 minutes to a stirred mixture of sodium methoxide (4.32 g.), N-(2-mercaptoethyl)phthalimide (16.6 g.) and methanol (100 ml.), and the mixture stirred for 1 hour after the addition was complete and then evaporated to dryness. The residue was partitioned between 1N hydrochloric acid and ethyl acetate, and the aqueous phase separated and neutralised by the addition of sodium bicarbonate. The mixture was extracted with ethyl acetate and the extracts dried and evaporated to dryness, and the residue was recrystallised from acetonitrile to give 4-amino-2-[(2-phthalimidoethyl)thiomethyl)pyrimidine, m.p. 131°-133°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04604465 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-c286f2be7c49455aad01d46e93ca62d8 |
| Source note | uspto-grants-1986_08 |