HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096214Generated: November 2, 2026
Sodium hydride → (Rac)-4-(tert-butyl-dimethyl-silanyloxy)-2-[7-oxo-4-(3-trifluoromethyl-phenyl)-[1,4]diazepan-1-yl]-butyric acid methyl ester
https://huagongshe.com/reaction/1096214
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 1-(3-Trifluoromethyl-phenyl)-[1,4]diazepan-5-one | HCID 21754509 | — |
| Reactant | (Rac)-4-(tert-butyl-dimethyl-silanyloxy)-2-iodo-butyric acid methyl ester | HCID 87149689 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (Rac)-4-(tert-butyl-dimethyl-silanyloxy)-2-[7-oxo-4-(3-trifluoromethyl-phenyl)-[1,4]diazepan-1-yl]-butyric acid methyl ester | HCID 66783316 | 217.3% |
Reaction Steps
A solution of 1.60 g (1.94 mmol) of 1-(3-trifluoromethyl-phenyl)-[1,4]diazepan-5-one in 15 ml of DMF was treated at 0° C. with 0.33 g (7.44 mmol) of NaH (55% dispersion in oil). After 20 min at this temperature, the suspension was warmed to RT and added to a cooled solution (0° C.) of 2.33 g (6.50 mmol) of (rac)-4-(tert-butyl-dimethyl-silanyloxy)-2-iodo-butyric acid methyl ester (intermediate 1) in 15 ml of DMF. The solution was stirred 6 h at 0° C. and neutralized with cold 10% aq. KH2PO4 solution and extracted with Et2O (3×). The organic phases were washed with 10% aq. KH2PO4 solution, dried over Na2SO4 evaporated and purified by flash silica gel column (CH2Cl2:Et2O 4:1 to 2:1) to yield 2.06 g (68%) of the title compound as light yellow oil. MS: 489.2 (MH+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08138175B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-71910e5679614fa8921bc7053889490f |
|---|
| Source note | uspto-grants-2012_03 |
|---|