HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486916Generated: October 30, 2026
Diisopropylethylamine → Ethyl 6-bromo-4-(oxan-4-ylamino)quinoline-3-carboxylate
https://huagongshe.com/reaction/1486916
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Aminotetrahydropyran | HCID 419223 | — |
| Reactant | Ethyl 6-bromo-4-chloroquinoline-3-carboxylate | HCID 2764138 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Ethyl 6-bromo-4-(oxan-4-ylamino)quinoline-3-carboxylate | HCID 118498649 | 96.9% |
Reaction Steps
On a larger scale, ethyl 6-bromo-4-chloroquinoline-3-carboxylate (2196 g, (1976 g active), 6.28 mol) was charged to the vessel with DMA (16 L). Tetrahydro-2H-pyran-4-amine (1224 g, 12.10 mol) was added over 10 minutes with an observed exotherm of 21-27° C. DIPEA (3.5 L, 20.09 mol) was added with no observed exotherm. The mixture was heated to 75-85° C. and the resulting solution stirred for 18.5 h at 80° C. HPLC indicated consumption of starting material and 99.2% product. The reaction was cooled to 50° C. and then poured into water (50 L). The resulting suspension was stirred for 2 h at r.t. and the solids isolated by filtration, washing with water (8 L then 2×4 L). The solid was dried under vacuum at 40° C. for 55 h to give 2307 g of desired material. Analytical data was consistent with that obtained from previous batches.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428503B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-497104888776471e99cb150086558a20 |
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| Source note | uspto-grants-2016_08 |
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