HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42348Generated: October 26, 2026
Diisopropylethylamine → HCID 178461982, compound
https://huagongshe.com/reaction/42348
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Reactant | (R)-4-(1-aminoethyl)-N-tert-butylbenzenesulfonamide | HCID 28714635 | — |
| Reactant | HCID 178517814 | HCID 178517814 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 178461982 | HCID 178461982 | 162.3% |
Reaction Steps
A mixture of 2-chloro-6-(4-fluorophenyl)pyrido[3,2-d]pyrimidin-4-ol (377 mg), (R)-4-(1-aminoethyl)-N-tert-butylbenzenesulfonamide (456 mg) and DIEA (243 ml) in NMP (4 ml) was heated at 120° C. overnight. The reaction mixture was then added to H2O/ACN (9:1) with vigorous stirring and extracted with EtOAc. The organic layer was dried and concentrated to give 1.1 g crude (R)—N-tert-butyl-4-(1-(6-(4 fluorophenyl)-4-hydroxypyrido[3,2-d]pyrimidin-2-ylamino)ethyl)benzenesulfonamide as golden brown oil, which was used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536187B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-d2f8bc44125c4c279e602f75ded9a355 |
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| Source note | uspto-grants-2013_09 |
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