HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403432Generated: November 1, 2026
(3-Amino-4-methylphenyl)boronic acid → HCID 66617799, compound
https://huagongshe.com/reaction/2403432
Participants
| Role | Name | HCID | Charge |
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| Reactant | (3-Amino-4-methylphenyl)boronic acid | HCID 2737803 | — |
| Reactant | 4-(2-Chloro-6-((4-methylpiperazin-1-yl)methyl)thieno[3,2-d]pyrimidin-4-yl)morpholine | HCID 57420338 | — |
| Product | HCID 66617799 | HCID 66617799 | — |
Reaction Steps
2-Chloro-6-(4-methyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine was reacted with 3-amino-4-methylbenzeneboronic acid in general procedure A. Purification by flash chromatography on silica yielded 2-Methyl-5-[6-(4-methyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-2-yl]-phenylamine. To a solution of 2-Methyl-5-[6-(4-methyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-2-yl]-phenylamine (154 mg) in chloroform (10 ml) and acetic acid (2 ml) was added isoamyl nitrite (55 μL). The reaction mixture was stirred at room temperature for 3 days. The reaction mixture was diluted with chloroform and washed with a 50/50 mixture of saturated sodium bicarbonate solution and brine, dried (MgSO4) and the solvents were removed in vacuo to give a crude residue. This was purified by flash chromatography to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802670B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-f633efa634b64cc6baa56c762f3f3172 |
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| Source note | uspto-grants-2014_08 |
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