HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418419Generated: November 2, 2026
4-Methylmorpholine → HCID 131720087, compound
https://huagongshe.com/reaction/1418419
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Proline benzyl ester hydrochloride | HCID 2733413 | — |
| Reactant | Boc-Met(O2)-OH | HCID 7017894 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131720087 | HCID 131720087 | — |
Reaction Steps
N-Boc-L-methionine sulfone-L-proline-O-benzyl ester was prepared by adding to a solution of N-Boc-L-methionine sulfone (14.0 g, 50.0 mmole) in dichloromethane (150 mL) at 0° C., HOBt (10.1 g, 75 mmole) followed by DCC (11.33 g, 55.0 mmole). The mixture was stirred for 10 minutes, and then L-proline benzyl ester hydrochloride salt (50.0 mmole, 12.0 g) was added followed by NMM (100 mmole, 10.9 mL). The resulting mixture was stirred in an ice bath and allowed to come to room temperature over 12 hours. The mixture was filtered to remove dicyclohexylurea and ethyl acetate (300 mL) was added. The organic phase was then added to a separatory funnel and washed with saturated aqueous sodium bicarbonate, brine and then 1M aqueous HCl. The organic phase was dried over magnesium sulfate and then filtered. The organic phase was then reduced on a rotary evaporator under vacuum and then on a high vacuum line to remove traces of solvent to provide 23.5 g of a white solid (100%). Rf=0.34 (silica, 5:95 methanol/chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05883107 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-16e92469f9324c4b93cebc86cbf7115d |
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| Source note | uspto-grants-1999_03 |
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