HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253605Generated: October 26, 2026
Ethanaminium, N,N,N-triethyl-, fluoride (1:1) → Methyl 2-((S)-(3-chlorophenyl)((R)-4-((2S,3R)-3-hydroxy-4-(methylamino)-1-(tetrahydro-2H-pyran-4-yl)butan-2-ylcarbamoyl)morpholin-2-yl)methoxy)ethylcarbamate
https://huagongshe.com/reaction/253605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanaminium, N,N,N-triethyl-, fluoride (1:1) | HCID 69582 | — |
| Reactant | HCID 66861750 | HCID 66861750 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-((S)-(3-chlorophenyl)((R)-4-((2S,3R)-3-hydroxy-4-(methylamino)-1-(tetrahydro-2H-pyran-4-yl)butan-2-ylcarbamoyl)morpholin-2-yl)methoxy)ethylcarbamate | HCID 16752763 | 12.4% |
Reaction Steps
A 10 mL flask was charged with methyl 2-((S)-(3-chlorophenyl)((R)-4-((2S,3R)-3-hydroxy-4-(N-methyl-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)-1-(tetrahydro-2H-pyran-4-yl)butan-2-ylcarbamoyl)morpholin-2-yl)methoxy)ethylcarbamate (30 mg, 0.043 mmol) dissolved in MeCN (4 mL) and Et4NF (14 mg, 0.094 mmol) was added. The mixture was stirred for 0.5 h under reflux. After stirring, it was monitored by HPLC until the reaction ended. The solution was concentrated in vacuo and purified by HPLC to give the target compound (2.97 mg, 12%). 1H NMR (MeOD) 1.27-1.30 (m, 2H), 1.32-1.40 (m, 2H), 1.51-1.62 (m, 2H), 1.65-1.80 (m, 2H), 2.70 (s, 3H), 1.75-1.90 (m, 2H), 1.90-3.10 (m, 4H), 3.65 (s, 3H), 3.80-3.95 (m, 5H), 4.05-4.20 (m, 1H), 4.30 (m, 1H), 7.25-7.40 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07872028B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-30caf40a8ac34126bfc62f556e4938bb |
|---|
| Source note | uspto-grants-2011_01 |
|---|