HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068877Generated: November 1, 2026
4-Methylmorpholine → HCID 178522644, compound
https://huagongshe.com/reaction/1068877
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 1,3-Dioxaindane-4-carboxylic acid | HCID 304832 | — |
| Reactant | HCID 178509242 | HCID 178509242 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178522644 | HCID 178522644 | — |
Reaction Steps
Under a nitrogen atmosphere, 320 μl (2.9 mmol) of NMM and 210 1 (1.6 mmol) of isobutyl chloroformate are added at −20° C. to 250 mg (1.5 mmol) of 2,3-methylenedioxybenzoic acid [for preparation see: Chem. Ber. 104 (1971) 2347] in 3.2 ml of THF and then stirred for 45 min. 378 mg (1.45 mmol) of 3-amino-4-(3-chloro-phenylamino)-1H-pyrazolo-[3,4-d]pyrimidine (see Step 1.6) are then added and the reaction mixture is allowed to rise to RT and is stirred for 1 hour to complete the reaction. The reaction mixture is poured into 100 ml of water and stirred for 1 hour, and the crude product is filtered off and washed with water and ethanol. Dissolution in 3 ml of DMSO at =110° C., cooling, filtering and washing with ethanol yield 4-(3chloro-phenylamino)-3-(2,3-methylenedioxy-benzoylamino)-1H-pyrazolo[3,4-d]pyrimidine; HPLC:tRet(grad20-100/20)=16.5; FAB-MS: (M+H)+=409.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251911B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-e31252d2d8c445639500f69d5fb1e5c5 |
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| Source note | uspto-grants-2001_06 |
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