HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 10076306, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methylnicotinic acid | HCID 643373 | — |
| Reactant | 3-Cyclopropylmethyl-8-[4-(methylamino)-benzyl]-1-(2-fluorobenzyl)-3,7-dihydropurine-2,6-dione | HCID 21891691 | — |
| Product | HCID 10076306 | HCID 10076306 | 34% |
Reaction Steps
This compound was prepared by a method similar to that described in example 79 except that 2-methylnicotinic acid (Aldrich) was used in place of N-acetyl-6-amino-2-pyridine carboxylic acid, N-bromosuccinimide was used in place of N-chlorosuccinimide, the reaction was performed using 0.66 equivalents of 3-cyclopropylmethyl-8-[4-(methylamino)-benzyl]-1-(2-fluorobenzyl)-3,7-dihydropurine-2,6-dione and 1 equivalent of triethylamine was added as the final reagent to the reaction mixture. Purification was performed by chromatography using silica eluted with 95:5 ethyl acetate/methanol to give the product as a light brown solid (34%). MS, M+H)=553.2361.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135475B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-a3f58d23188d4841b3f5bb8303b5f7c1 |
| Source note | uspto-grants-2006_11 |