HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-({4-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]phenyl}formamido)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | N-Fluorenylmethoxycarbonyl-I2-alanine | HCID 2724630 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | 4-[(9H-fluoren-9-yl-methoxycarbonylamino)methyl]benzoic acid | HCID 67483812 | — |
| Solvent | N,N-Diethyl-2-propanamine | HCID 521913 | — |
| Product | 3-({4-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]phenyl}formamido)propanoic acid | HCID 22502198 | — |
Reaction Steps
To the above resin bound Fmoc β-alanine was added 500 μL of a 20% solution of piperidine in DMF. Upon shaking 30 min, the resin was drained and washed with 1 mL DMF containing 1-hydroxybenzotriazole (50 mg/mL) and DMF (2×1 mL). Then 200 μmol 4-[(9H-fluoren-9-yl-methoxycarbonylamino)methyl]benzoic acid (74.2 mg) dissolved in a mixture of 430 μL DMF and 70 μL diethylisopropylamine was added followed by 200 μmol bromo-tris-pyrrolidinophosphonium hexafluorophosphate (PyBrOP, 93 mg) dissolved in 500 μL DMF. The mixture was shaken for 4 hours at 25° C. followed by filtration and washing of the resin with 3×1 mL DMF.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06503949B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-98831ac4c99f41409baa9aea4ac6052a |
| Source note | uspto-grants-2003_01 |