HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523191Generated: October 25, 2026
Diisopropylethylamine → HCID 86683260, compound
https://huagongshe.com/reaction/523191
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (4R)-4-Hydroxy-L-proline methyl ester | HCID 7015125 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 86683261 | HCID 86683261 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86683260 | HCID 86683260 | 53.4% |
Reaction Steps
To a solution of (3R)-2-(tert-butoxycarbonylamino)-3-ethyl-5-methylnon-8-enoic acid (2.0 g, 6.4 mmole) in dichloromethane (20 mL) was added DIPEA (1.93 mL, 19.2 mmole) and HATU (2.42 g, 6.38 mmole) followed by (2S,4R)-methyl 4-hydroxypyrrolidine-2-carboxylate (1.15 g, 6.38 mmole) at room temperature. The reaction mixture was stirred at room temperature for 2 h. The reaction mass was diluted with DCM and washed with water. The organic layer was dried over anhydrous Na2SO4; filtered; then concentrated under reduced pressure to get crude compound as mixture of diastereomers. The material was subjected to SFC purification to afford (2S,4R)-methyl 1-((2S,3R)-2-(tert-butoxycarbonylamino)-3-ethyl-5-methylnon-8-enoyl)-4-hydroxypyrrolidine-2-carboxylate (1.5 g, 53%). MS: MS m/z 441.6 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334279B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-c986ea5d580242699b99239ec61a45b1 |
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| Source note | uspto-grants-2016_05 |
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