HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951192Generated: October 26, 2026
(4-Methoxy-benzyl)-[4-methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-yl]-amine → 4-Methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-ylamine
https://huagongshe.com/reaction/1951192
Participants
| Role | Name | HCID | Charge |
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| Reactant | (4-Methoxy-benzyl)-[4-methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-yl]-amine | HCID 86610335 | — |
| Solvent | Trifluoroacetic acid water | HCID 22392675 | — |
| Product | 4-Methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-ylamine | HCID 86610336 | — |
Reaction Steps
A solution comprising (4-methoxy-benzyl)-[4-methyl-5-(2-morpholin-4-yl-pyrimidin-4-yl)-thiazol-2-yl]-amine (25c) (0.45 g, 1.13 mmol) in trifluoroacetic acid:water (95:5) (10 ml) is heated at 75° C. for days. The solvent is removed in vacuo and the crude residue is dissolved in ethyl acetate. The pH is adjusted to pH12 using 2N sodium hydroxide and the layers are separated. The aqueous layer is extracted with ethyl acetate (2×30 ml). The organic portions are combined and washed with brine (50 ml), dried over MgSO4 and concentrated in vacuo to yield the titled compound as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404684B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-8c7f8a191e05474a866482fb25528157 |
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| Source note | uspto-grants-2013_03 |
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