HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → 2-[(2-Chloroacetyl)amino]-6-methylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | 6-Methylanthranilic acid | HCID 151210 | — |
| Product | 2-[(2-Chloroacetyl)amino]-6-methylbenzoic acid | HCID 10633076 | — |
Reaction Steps
2-amino-6-methylbenzoic acid is reacted with 2-chloroacetyl chloride to produce the 2-(-2-chloroacetamido)-6-methylbenzoic acid. Reaction with o-toluidine and phosphoryl trichloride yields the cyclized intermediate. Further reaction with diBOC-protected adenine give the BOC protected product, which is deprotected resulting in 2-((6-amino-9H-purin-9-yl) methyl)-5-methyl-3-o-tolylquinazolin-4(3H)-one (2c).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691829B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-27ff6d6b3d624ec1ab6476d8666e098d |
| Source note | uspto-grants-2014_04 |