HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828653Generated: October 31, 2026
4-Methylmorpholine → HCID 23591746, compound
https://huagongshe.com/reaction/1828653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Benzyloxycarbonylglycine | HCID 14349 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | tert-Butyl (3-aminopropyl)carbamate | HCID 2735700 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23591746 | HCID 23591746 | — |
Reaction Steps
To 3 grams of (3-Amino-propyl)-carbamic acid tert-butyl ester in 15 ml of dimethylformamide was added 3 grams of N-benzyloxycarbonyl glycine, 4.7 mL of N-methylmorpholine and 5.06 grams of TBTU. The reaction was cooled to 0 degrees C. for 30 minutes then allowed to stir at room temperature overnight. The volatiles were removed under reduced pressure and the resulting material was dissolved in ethyl acetate and washed with 10% citric acid. The aqueous was extracted an additional two times with ethyl acetate, combined and washed with water, saturated aqueous sodium bicarbonate, water, brine and dried over MgSO4. The volatiles were removed under reduced pressure and the resulting material was crystallized from EtOAc/hexane affording 4.55 grams of the desired product as a tan solid. LRMS found 388.3=(M+Na)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07060248B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-ca7237c46c954944bc26f61158ff7e2c |
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| Source note | uspto-grants-2006_06 |
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