HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158341Generated: October 27, 2026
Methylamine → (3R*,4R*)-3-({Isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-4-methylaminomethyl-pyrrolidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1158341
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (3S*,4R*)-3-formyl-4-({isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 59512275 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3R*,4R*)-3-({Isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-4-methylaminomethyl-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 59512501 | — |
Reaction Steps
To a solution of (3S*,4R*)-3-formyl-4-({isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (150 mg, 0.304 mmol) and magnesium sulfate (92 mg, 0.373 mmol) in THF (4 mL), methylamine (1.52 mL, 3.044 mmol, 2M in THF) is added. The solution is stirred at RT overnight under nitrogen atmosphere and NaBH4 (23 mg, 0.608 mmol) is added. The resulting mixture is stirred for 1 h and the excess reducing agent quenched with water, CH2Cl2 is added and the reaction mixture is poured into an aqueous saturated solution of NaHCO3. The organic layer is separated and the aqueous phase extracted twice with CH2Cl2, dried over Na2SO4, filtered, and concentrated in vacuo. The crude material is purified by flash chromatography on silica gel (eluent: CH2Cl2/MeOH 100:0 to 95:5+1% NH4OH ) to give the title product. TLC, Rf (CH2Cl2/MeOH 95:5)=0.05. MS (LC-MS) [M−H]+=508.1. tR (HPLC, Nucleosil C18 column, 10-100% CH3CN/H2O/5 min, 100% CH3CN/3 min, CH3CN and H2O containing 0.1% TFA, flow: 1.5 ml/min): 4.53 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807709B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-f19e11325e144320ad0c76b64dd40892 |
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| Source note | uspto-grants-2010_10 |
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