HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643067Generated: October 30, 2026
Trifluoroacetic acid → methyl (1S)-2-methyl-1-({2-[4-(2-pyridinyl)benzyl]hydrazino}carbonyl)propylcarbamate
https://huagongshe.com/reaction/643067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one | HCID 4293995 | — |
| Reactant | tert-Butyl 2-(4-(pyridin-2-yl)benzyl)hydrazinecarboxylate | HCID 9796325 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl (1S)-2-methyl-1-({2-[4-(2-pyridinyl)benzyl]hydrazino}carbonyl)propylcarbamate | HCID 91615834 | 47% |
Reaction Steps
A solution of Example 4B (0.18 g, 0.6 mmol) in dichloromethane:trifluoroacetic acid (4 mL, 1:1) was stirred at 25° C. for 1 h, and the solvents were evaporated. This material was dissolved in THF (1 mL) and treated with diisopropylethyl amine (0.31 mL, 3 equivalents), DEPBT (0.36 g, 2 equivalents), and Example 18A (0.105 g, 1 equivalent), stirred at 25° C. for 3 h. The mixture was partitioned between dichloromethane and 10% sodium carbonate, the organic layer was separated, washed with brine, dried over sodium sulfate, filtered and the solvents were evaporated. The crude residue was purified using 2% methanol/chloroform to give 0.1 g (47%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696226B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-78d62214a5224b799cfb2c7563973491 |
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| Source note | uspto-grants-2010_04 |
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