HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665544Generated: October 29, 2026
Phenyl 4-carbamoylphenylcarbamate → 4-({[4-(4-{4-[(Methylcarbamoyl)amino]phenyl}-6-morpholin-4-yl-1,3,5-triazin-2-yl)phenyl]carbamoyl}amino)benzamide
https://huagongshe.com/reaction/1665544
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenyl 4-carbamoylphenylcarbamate | HCID 60631229 | — |
| Reactant | 1-(4-(4-(4-Aminophenyl)-6-morpholino-1,3,5-triazin-2-yl)phenyl)-3-methylurea | HCID 67438523 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-({[4-(4-{4-[(Methylcarbamoyl)amino]phenyl}-6-morpholin-4-yl-1,3,5-triazin-2-yl)phenyl]carbamoyl}amino)benzamide | HCID 66585526 | 5.3% |
Reaction Steps
To a solution of 1-(4-(4-(4-aminophenyl)-6-morpholino-1,3,5-triazin-2-yl)phenyl)-3-methylurea (0.6 g, 1.5 mmol) and triethylamine(4-5 mL) in dry DMF (10 mL), phenyl 4-carbamoylphenylcarbamate (1.15 g, 4.5 mmol).) was added at room temperature and mixture was heated to 90° C. for 10 hours under nitrogen atmosphere. After cooling to room temperature reaction mixture was quenched with ice water and resulting solid was filtered to get crude product. Crude product was purified by Preparative HPLC to give 4-({[4-(4-{4-[(methylcarbamoyl)amino]phenyl}-6-morpholin-4-yl-1,3,5-triazin-2-yl)phenyl]carbamoyl}amino)benzamide (45 mg, 5.3% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039469B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-28543dcf22484f60b50117ebff7bfbd1 |
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| Source note | uspto-grants-2011_10 |
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