HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486752Generated: October 26, 2026
Sodium Bicarbonate → HCID 118521983, compound
https://huagongshe.com/reaction/1486752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 5-[(tert-Butoxycarbonyl)amino]pyridine-2-carboxylic acid | HCID 28875521 | — |
| Reactant | 1-(3-Amino-benzyl)-piperidine-4-carboxylic acid tert-butylamide | HCID 86706525 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118521983 | HCID 118521983 | 58% |
Reaction Steps
A solution of 5-[[(1,1-dimethylethoxy)carbonyl]amino]-2-pyridinecarboxylic acid (1 g, 4.11 mmol) in DCM (30 mL) is treated successively with 1-(3-amino-benzyl)-piperidine-4-carboxylic acid tert-butylamide (1.309 g, 4.525 mmol), EDC-HCl (1.577 g, 8.227 mmol), DMAP (75 mg, 0.62 mmol). The RM is stirred at RT for 18 h. DCM (10 mL) and aq. sat. NaHCO3 solution (30 mL) are added and the organic phase is extracted twice with DCM (2×20 mL). The combined organic layers are dried over MgSO4, filtered and evaporated. The residue is purified by flash chromatography on silica gel using a gradient of DCM/MeOH from DCM to DCM/MeOH 9:1. After concentration of the product containing fractions, the title compound (1.21 g, 58%) is obtained as a beige powder LC-MS A: tR=0.75 min; [M+H]+=510.23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428456B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-9c2e5d3e675f45b9b7b6a07d468f933c |
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| Source note | uspto-grants-2016_08 |
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