HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5H-Pyrrolo3,2-dpyrimidin-2-amine, 4-(phenylmethoxy)-5-(phenylmethoxy)methyl- | HCID 22222458 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl- | HCID 11812212 | 94.3% |
Reaction Steps
A solution of 2-amino-4-benzyloxy-5-N-benzyloxymethylpyrrolo[3,2-d]pyrimidine (1.0 g) in methylene chloride (30 mL) was stirred in an ice bath while N-bromosuccinimide (0.5 g) was added portion-wise. The solution was concentrated and chromatography afforded 2-amino-4-benzyloxy-5-N-benzyloxymethyl-7-bromopyrrolo[3,2-d]pyrimidine (1.15 g) as a white solid. 13C NMR (CDCl3) δ 158.8, 157.2, 150.9, 137.3, 136.6, 131.8, 129.0, 128.8, 128.6, 128.5, 128.3, 127.9, 111.3, 90.3, 77.8, 70.7, 68.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07211677B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-cb3dc5fcddce4e518807766156019916 |
| Source note | uspto-grants-2007_05 |