HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786717Generated: October 30, 2026
Imatinib → N-(4-Methyl-3-nitro-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide
https://huagongshe.com/reaction/1786717
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imatinib | HCID 5291 | — |
| Reactant | 4-Methyl-3-nitroaniline | HCID 8390 | — |
| Reactant | Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate | HCID 782222 | — |
| Product | N-(4-Methyl-3-nitro-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide | HCID 29984087 | — |
Reaction Steps
U.S. Pat. No. 5,521,184 and application WO 03/066613 describe several synthetic routes for preparing Imatinib. One synthetic process, described in Scheme 1, comprises reacting 4-(4-methyl-piperazin-1-ylmethyl)-benzoic acid methyl ester with 3-nitro-4-methyl-aniline to obtain N-(4-methyl-3-nitrophenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide, which is subsequently reduced to obtain N-(3-amino-4-methyl-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide. The latter is reacted with cyanamide (NH2CN) in a mixture of concentrated hydrochloric acid solution and n-butanol to produce N-(3-guanidino-4-methyl-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide, which is subsequently reacted with 3-dimethylamino-1-pyridin-3-yl-propenone to obtain Imatinib.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507821B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-416ea1cf0f1a47d29ae88e86e018323e |
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| Source note | uspto-grants-2009_03 |
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