HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111310Generated: November 2, 2026
4-Methylmorpholine → HCID 18642403, compound
https://huagongshe.com/reaction/1111310
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Benzyloxycarbonyl-L-proline | HCID 101987 | — |
| Reactant | HCID 22152159 | HCID 22152159 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18642403 | HCID 18642403 | — |
Reaction Steps
A solution was prepared by dissolving 249 mg of N-carbobenzoxy-L-proline and 101.0 mg of N-methylmorpholine in 5 ml of dry tetrahydrofuran and cooling to a temperature of -15° C. The solution was mixed with 136.6 mg of isobutyl chloroformate and the mixture was stirred at a temperature of -15° C. to -10° C. for 2 minutes. Then, a solution of 238 mg of 4-amino-2-carboisopropoxyaminobenzoic acid and 101.2 mg of N-methylmorpholine in 2 ml of dry tetrahydrofuran was added dropwise to the above-mentioned mixture. The resultant reaction mixture was stirred at a temperature of -15° C. to -10° C. for one hour, gradually heated to room temperature, and then stirred at room temperature for 18 hours. The resultant deposit generated in the reaction mixture was removed by filtration, the filtrate was concentrated under a reduced pressure, and an oily yellow substance was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04980287 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-a7054b498dba4f389f580038aa0fa1ed |
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| Source note | uspto-grants-1990_12 |
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