HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241405Generated: October 30, 2026
2-Bromo-N-cyclopropylacetamide → 2-(4-{6-[(5-Cyano-1,3-thiazol-2-yl)amino]pyrimidin-4-yl}piperazin-1-yl)-N-cyclopropyl-acetamide
https://huagongshe.com/reaction/1241405
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromo-N-cyclopropylacetamide | HCID 16757560 | — |
| Reactant | 2-(6-(Piperazin-1-yl)pyrimidin-4-ylamino)thiazole-5-carbonitrile | HCID 21934630 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(4-{6-[(5-Cyano-1,3-thiazol-2-yl)amino]pyrimidin-4-yl}piperazin-1-yl)-N-cyclopropyl-acetamide | HCID 21934698 | — |
Reaction Steps
12-3 (0.2 g, 0.39 mmol) and 2-bromo-N-cyclopropylacetamide 38-1 (0.069 g, 0.39 mmol) were suspended in chloroform/2M Na2CO3 in a sealed tube and heated in a Smith Personal Chemistry microwave reactor at 100° C. for 20 minutes. The solid was then filtered off and purified on a silica column to afford 38-2. Hi-Res MS: calc: 385.1554 found: 385.1548. 1H-NMR (CD3OD): 8.39(s, 1H); 7.99(s, 1H); 6.14(s, 1H); 3.68(m, 4H); 3.05(s, 2H); 2.70(m, 1H); 2.58(m, 4H); 0.75(m, 2H); 0.55(m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115597B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-5016891323dc491ca8501aece2c21615 |
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| Source note | uspto-grants-2006_10 |
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