HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654587Generated: October 30, 2026
4-Methylmorpholine → HCID 131718970, compound
https://huagongshe.com/reaction/1654587
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | (2S)-2-(((benzyloxy)carbonyl)amino)-3,3-dimethylbutanoic acid | HCID 9899995 | — |
| Reactant | L-Leucine, ethyl ester, hydrochloride (1:1) | HCID 11658447 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131718970 | HCID 131718970 | 100.3% |
Reaction Steps
Z-Tle (15.6 g, 59.1 mmol), Leu-OEt HCl (11.56 g, 59.1 mmol), and N-methyl morpholine (NMM) (12.75 mL) are mixed with 45 mL of DMF and a cloudy suspension forms. The mixture is cooled to 0° C. and treated with TBTU (19.1 g, 59.48 mmol), then stirred at 0° C. for 15 minutes, then removed from the cold bath and stirred for 1.5 hours. The mixture is poured into 500 mL of a saturated solution of sodium carbonate which is then extracted with two 350 mL portions of ethyl acetate. The combined organic extracts are washed with 500 mL of 1 M KHSO4 water and brine and then dried over sodium sulfate. The solvents are removed to give Z-Tle-Leu-OEt (24.1 g). FABMS M+1 407
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05407916 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-a62e2435ec1348bbb0eec7feef7a588f |
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| Source note | uspto-grants-1995_04 |
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