HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine chloride → 2-Amino-6-ethylamino-4-iodopyrimidine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | 2-Amino-6-ethylaminopyrimidine | HCID 54461799 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Amino-6-ethylamino-4-iodopyrimidine hydrochloride | HCID 86628415 | 98% |
Reaction Steps
To a solution of 2-amino-6-ethylaminopyrimidine (98 g, 0.64 mol) in methanol (1.6 L) was added ICl (115.0 g, 0.71 mol) in a small portion at 15° C. Then the reaction mixture was stirred at room temperature for 3 h (monitored by LC/MS). After evaporation of solvent by rotary evaporator, the residue was triturated with acetone. 2-amino-6-ethylamino-4-iodopyrimidine hydrochloride (188.5 g, 93% isolated yield) was obtained by vacuum filtration and drying. 1H NMR (400 MHz, CD3OD) δ 3.58 (q, 2H), 2.14 (s, 3H), 1.11 (t, 3H); MS (EI) for C7H11N4ClI: 279.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513266B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-aa42385037594830b7e2c9c6c969d15b |
| Source note | uspto-grants-2013_08 |