HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808412Generated: October 30, 2026
Diisopropylethylamine → HCID 56949456, compound
https://huagongshe.com/reaction/1808412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Morpholineacetic acid | HCID 438968 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate | HCID 66825994 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 56949456 | HCID 56949456 | — |
Reaction Steps
A suspension of 2-morpholinoacetic acid (16 mg, 0.11 mmol), PyBOP® (57 mg, 0.11 mmol), DIEA (96 μL, 0.55 mmol) in CH2Cl2 (0.5 mL) was stirred at RT for 10-15 minutes. This solution of activated acid was added to a suspension of tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate 0 (100 mg, 0.22 mmol) and CH2Cl2 (1 mL). The reaction mixture was stirred at RT for 1.5 h. Activated another 0.5 equivalent of the acid as described above and it was once again added to the reaction mixture and stirred for 1.5 h. Added two more 0.5 equivalents of activated acid while stirring 1.5 hr between each addition. Diluted with more CH2Cl2 and extracted with H2O (3×). Organic layer was dried under Na2SO4 and concentrated in vacuo to give the desired oil product tert-butyl 5-(2-(3-(2-morpholinoacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357693B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-10a87cb967c249409c9f83e6d7a51885 |
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| Source note | uspto-grants-2013_01 |
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