HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649843Generated: November 1, 2026
Triethylamine → 2-Amino-4-[4-(diphenylmethoxy)piperidinomethyl]thiazole
https://huagongshe.com/reaction/1649843
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Thiazolamine, 4-(chloromethyl)-, hydrochloride (1:1) | HCID 73228 | — |
| Reactant | 4-Benzhydryloxypiperidine | HCID 3017584 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Amino-4-[4-(diphenylmethoxy)piperidinomethyl]thiazole | HCID 19854937 | 70.4% |
Reaction Steps
A stirred mixture of 2-amino-4-chloromethylthiazole hydrochloride (0.7 g), 4-(diphenylmethoxy)piperidine (0.78 g) and triethylamine (1.82 ml) in N,N-dimethylformamide (7.8 ml) was heated at 40° C. to 45° C. for 5 hours. After cooling to ambient temperature, the reaction mixture was filtered. The filtrate was poured into water (50 ml) and extracted with ethyl acetate (80 ml×2). The extract was washed with a saturated aqueous solution of sodium chloride (30 ml) and dried over magnesium sulfate. The solvent was distilled off and the residue was subjected to column chromatography on silica gel (30 g) and eluted with a mixture of chloroform and methanol (10:1 V/V). The fractions containing the object compound were combined and concentrated under reduced pressure to give 2-amino-4-[4-(diphenylmethoxy)piperidinomethyl]thiazole (0.78 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04921887 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-a215d011ffc14004bdad469d90986a1b |
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| Source note | uspto-grants-1990_05 |
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