HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863917Generated: November 2, 2026
Hydrazine → Tert-butyl[(1r)-1-(2,5-difluorobenzyl)-3-hydrazino-3-oxopropyl]carbamate
https://huagongshe.com/reaction/1863917
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | (R)-b-(Boc-amino)-2,5-difluorobenzenebutanoic acid | HCID 11347588 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl[(1r)-1-(2,5-difluorobenzyl)-3-hydrazino-3-oxopropyl]carbamate | HCID 57973777 | — |
Reaction Steps
To a solution of 94.6 mg (0.3 mmol) of (3R)-3-[(tert-butoxycarbonyl)amino]-4-(2,5-difluorophenyl)butanoic acid (Intermediate 1) in 1.5 mL of anhydrous dichloromethane, stirred in an ice bath under protection from moisture, was added 0.0106 mL (10.8 mmol) of anhydrous 98% hydrazine. Then 91.8 mg of 1-hydroxybenzotriazole hydrate was added, followed by 63.4 mg (0.33 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) and finally 0.0574 mL (42.6 mg, 0.33 mmol) of N,N-diisopropylethylamine. After 15 minutes, an additional 0.0574 mL (42.6 mg, 0.33 mmol) of N,N-diisopropylethylamine was added. After 2 h, the mixture was removed from the ice bath and allowed to warm to room temperature, and precipitation gradually increased. After 22 h, the precipitated solid was collected on a filter, washed with small volumes of dichloromethane, and dried to give the title compound as a white solid, mp 168-169° C. LC-MS 230 (M+1-Boc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07625888B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-85ab867d9c0b463c9ce0b26068aa180f |
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| Source note | uspto-grants-2009_12 |
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