HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545002Generated: October 29, 2026
Acetic Anhydride → HCID 59851270, compound
https://huagongshe.com/reaction/545002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 56946380 | HCID 56946380 | — |
| Reactant | HCID 178506946 | HCID 178506946 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59851270 | HCID 59851270 | — |
Reaction Steps
To a solution of 2-(3,4-dimethoxy-phenylamino)-9-iodo-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-one (I-30) (0.60 g, 1.20 mmol) in dry DMF (8 mL) was added Ac2O (0.23 mL, 2.44 mmol), HCOOLi (0.19 g, 3.66 mmol), LiCl (0.155 g, 3.66 mmol), and Pd(OAc)2 (0.01 g, 0.06 mmol). Lastly, i-Pr2NEt (0.42 mL, 2.44 mmol) was added and the mixture heated for 16 h at 80° C. in a sealed tube. The reaction mixture was then diluted with CH2Cl2 (30 mL), and the organic layer was washed with H2O (3×30 mL), dried over MgSO4, filtered and concentrated in vacuo to give crude product as a yellow solid. The solid was treated with EtOAc and sonicated to provide a white solid which was collected by filtration to provide I-53 (0.33 g, 71%): HRMS Calcd. for C21H18N4O5: 407.1355, Found 407.1364.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935694B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-f3d57b05b70d44b58831dc7f56c385c2 |
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| Source note | uspto-grants-2011_05 |
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