HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623684Generated: October 30, 2026
Ethylamine → [3-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-5-ethylcarbamoyl-3H-[1,2,3]triazol-4-yl]-(4-morpholin-4-yl-phenyl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/623684
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 1-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-5-[tert-butoxycarbonyl-(4-morpholin-4-yl-phenyl)-amino]-1H-[1,2,3]triazole-4-carboxylic acid methyl ester | HCID 117677875 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [3-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-5-ethylcarbamoyl-3H-[1,2,3]triazol-4-yl]-(4-morpholin-4-yl-phenyl)-carbamic acid tert-butyl ester | HCID 117678067 | — |
Reaction Steps
EtNH2 (1.5 ml of a solution 2 M in MeOH) was added to 1-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-5-[tert-butoxycarbonyl-(4-morpholin-4-yl-phenyl)-amino]-1H-[1,2,3]triazole-4-carboxylic acid methyl ester (110 mg, 0.15 mmol) and the mixture was heated to 80° C. for 24 hours in a sealed tube. The solvent and the excess of amine were removed under reduced pressure and the residue was used in the next reaction without any purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09302998B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-bf880cc31ab24ef4973ce7a5f96fb46f |
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| Source note | uspto-grants-2016_04 |
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