HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820149Generated: October 26, 2026
2-Thiophenecarboxaldehyde, 5-chloro- → {4-[(5-Chloro-thiophen-2-ylmethyl)-amino]-2,6-dimethyl-phenyl}-carbamic acid propyl ester
https://huagongshe.com/reaction/1820149
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Thiophenecarboxaldehyde, 5-chloro- | HCID 81700 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Sodium chloride dihydrate | HCID 23713072 | — |
| Reactant | (4-Amino-2,6-dimethyl-phenyl)-carbamic acid propyl ester | HCID 68707091 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | {4-[(5-Chloro-thiophen-2-ylmethyl)-amino]-2,6-dimethyl-phenyl}-carbamic acid propyl ester | HCID 11508619 | 49% |
Reaction Steps
(4-Amino-2,6-dimethyl-phenyl)-carbamic acid propyl ester (84 mg) and 5-chloro-thiophene-2-carbaldehyde (48 uL) were dissolved in methanol (3 mL) and heated to 130° C. for 5 minutes in a sealed microwave process vial. Sodium cyanoborohydride (95 mg) was added and the reaction mixture was heated to 130° C. for 5 minutes in a sealed microwave process vial, followed by addition of water/brine (1:1, 3 mL). The product was extracted with ethyl acetate (3×3 mL) and the combined organic phases were washed with brine (5 mL), dried over magnesium sulfate and concentrated in vacuo. The crude product was purified by flash chromatography to furnish 66 mg (49% yield) of the title compound as an oil. LC-MS (m/z) 353 (MH+); tR=3.06, (UV, ELSD) 87%, 87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601870B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-efce2a94360740d0bc3b9cacfd4823b4 |
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| Source note | uspto-grants-2009_10 |
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