HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545003Generated: October 28, 2026
Diisopropylethylamine → HCID 59851365, compound
https://huagongshe.com/reaction/545003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 59851270 | HCID 59851270 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59851365 | HCID 59851365 | — |
Reaction Steps
To a solution of 2-(3,4-dimethoxy-phenylamino)-6-oxo-6,7-dihydro-5H-benzo[b]pyrimido[4,5-d]azepine-9-carboxylic acid (I-53) (75 mg, 0.18 mmol) in DMF (5 mL) was added N,N-diisopropylethylamine (0.10 mL, 0.55 mmol), TBTU (65 mg, 0.20 mmol), and tert-butyl 2-aminoethylcarbamate (35.5 mg, 0.22 mmol). The reaction stirred at 22° C. overnight. The reaction mixture was diluted with H2O, and the precipitate that formed was filtered, washed with H2O and dried to give I-71-a [MS m/z=549 (M+H)] which was carried on crude to the deprotection.
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-476a7b1b5e3f4239bf890065d6228327 |
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| Source note | uspto-grants-2011_05 |
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