HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73210Generated: October 30, 2026
Formaldehyde → HCID 178499314, compound
https://huagongshe.com/reaction/73210
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 178499313 | HCID 178499313 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 178499314 | HCID 178499314 | 85.7% |
Reaction Steps
To a stirred solution of 3-[(trans-4-methyl-cyclohexanecarbonyl)-piperidin-4-yl-amino]-thiophene-2-carboxylic acid methyl ester (1.0 g, 2.7 mmol), from step 3, in 1,2-dichloroethane (10 mL) was sequentially added aq. 37% HCHO solution (0.45 mL, 5.4 mmol) and NaBH(OAC)3 (2.86 g, 13.5 mmol) in one portion, stirred for over night, reaction was then quenched with aq. 10% NaOH solution, extracted with DCM. The combined organic extract was washed with brine, dried, and concentrated to obtain 3-[(trans-4-methyl-cyclohexanecarbonyl)-(1-methyl-piperidin-4-yl)-amino]-thiophene-2-carboxylic acid methyl ester (0.876 g, 85.5%) as a white solid. NMR 1H (CDCl3, 400 MHz): 7.54 (d, 1H), 6.86 (d, 1H), 4.7-4.6 (m, 1H), 3.85 (s, 3H), 2.9-2.7 (m, 2H), 2.22 (s, 3H), 2.15-1.1 (m, 14H), 0.8 (d, 3H), 0.75-0.5 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829030B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-dd813195862548558d15f2e7f67ee22f |
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| Source note | uspto-grants-2014_09 |
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