HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639635Generated: October 28, 2026
1,2-Dichloroethane → HCID 178452920, compound
https://huagongshe.com/reaction/1639635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 4-(Morpholinomethyl)benzene-1,2-diamine | HCID 25193309 | — |
| Reactant | HCID 178452921 | HCID 178452921 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178452920 | HCID 178452920 | 96% |
Reaction Steps
A mixture of 4-tert-butoxycarbonylamino-1H-pyrazole-3-carboxylic acid (10.0 g, 44.1 mmol), 4-morpholin-4-ylmethyl-benzene-1,2-diamine (10.0 g, 48.5 mmol), EDC (10.14 g, 52.9 mmol) and HOBt (7.15 g, 52.9 mmol) in DMF (150 mL) was stirred at ambient temperature for 20 h and then the majority of the solvent removed in vacuo. The residue was partitioned between EtOAc (150 mL) and saturated aqueous NaHCO3 (150 mL), the layers separated and the organic portion washed with brine, dried over MgSO4 and reduced in vacuo to give [3-(2-amino-4-morpholin-4-ylmethyl-phenylcarbamoyl)-1H-pyrazol-4-yl]-carbamic acid tert-butyl ester (17.6 g, 96%) as a brown solid. LC/MS analysis indicates product contains 15% of the di-amide. This shows at approx. 5% level in 1H NMR. Di-amide is cleaved in subsequent step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110573B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-701e895c8dd54581ad0b6bd67d5e748a |
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| Source note | uspto-grants-2012_02 |
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