HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693253Generated: October 31, 2026
Diisopropylethylamine → HCID 57827215, compound
https://huagongshe.com/reaction/1693253
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 57827362 | HCID 57827362 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57827215 | HCID 57827215 | — |
Reaction Steps
PyBOP (205 mg) was added to a solution of tert-butyl(±)-[(4aR*,6S*,7aS*)-7a-(5-amino-2-fluorophenyl)-6-ethoxy-4,4a,5,6,7,7a-hexahydrocyclopenta[d][1,3]thiazin-2-yl]carbamate (52 mg), the compound of Preparation Example 26-(2) (27.3 mg) and N,N-diisopropylethylamine (0.26 mL) in dichloromethane (5.2 mL). The mixture was stirred at room temperature for one hour. The reaction solution was poured into a saturated sodium bicarbonate solution, followed by extraction with ethyl acetate. The extract was washed with a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to obtain the title compound (45 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158620B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-05d015f1be4145fab35d7b6e815109f7 |
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| Source note | uspto-grants-2012_04 |
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