HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897666Generated: October 29, 2026
N,N-Diethylethylenediamine → HCID 22346964, compound
https://huagongshe.com/reaction/897666
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Diethylethylenediamine | HCID 60993 | — |
| Reactant | HCID 22346820 | HCID 22346820 | — |
| Product | HCID 22346964 | HCID 22346964 | — |
Reaction Steps
The representative procedure for amide formation was used in the reaction of methyl 2-[4-amino-3-(4-{[(2,3-dichlorophenyl)sulfonyl]amino}-3-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]acetate (0.035 g, 0.067 mmol) with N,N-diethylethylenediamine (1 mL). Purification by preparative HPLC (25 to 100% acetonitrile in 0.1 M aqueous ammonium acetate over 20 min at 21 mL/min using an 8μ Hypersil HS C18, 250×21 mm column, Rt 7.12-7.98 min) afforded N1-[2-(diethylamino)ethyl]-2-[4-amino-3-(4-{[(2,3-dichlorophenyl)sulfonyl]amino}-3-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]acetamide as an off-white solid (0.017 g, 0.028 mmol): 1H NMR (DMSO-d6, 400 MHz) δ 8.22 (s, 1H), 8.12 (br, 1H), 7.96 (d, 1H), 7.78 (d, 1H), 7.44 (t, 1H), 7.31 (m, 3H); 6.95 (br, 2H), 4.96 (s, 2H), 3.35 (m, 2H), 2.82 (m, 2H), 2.50 (m, 4H), 1.05 (t, 6H); MS: (M−H)− 607.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921763B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-6520d8e0194f4fdb9a42ec505c63d398 |
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| Source note | uspto-grants-2005_07 |
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