HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444674Generated: October 26, 2026
Gamma-Aminobutyric Acid → 4-(3-Adamantan-1-yl-ureido)butyric acid
https://huagongshe.com/reaction/444674
Participants
| Role | Name | HCID | Charge |
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| Reactant | Gamma-Aminobutyric Acid | HCID 119 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Isocyanatoadamantane | HCID 2059995 | — |
| Product | 4-(3-Adamantan-1-yl-ureido)butyric acid | HCID 11425995 | 100% |
| Product | 4-(3-Adamantan-1-yl-ureido)butyric Acid Methyl Ester | HCID 11437855 | — |
Reaction Steps
The title compound was prepared by a procedure described in J. Med. Chem. 2004, 47, 2110. To a suspension of 4-aminobutyric acid (2.79 g, 27.1 mmol) in DMF (40 mL) was added 1-adamantyl isocyanate (1.20 g, 6.77 mmol) at room temperature. The reaction mixture was stirred for 24 h. Then 1 N HCl aqueous solution (40 mL) was added into the reaction, and the mixture was stirred for 30 min. The solid crystalline product was filtered and washed with water (20 mL) and ethyl acetate (20 mL). The resulting solid was dried in a vacuum oven to give 1.90 g (100%) of 4-(3-adamantan-1-yl-ureido)butyric acid 822 as a white solid: 1H NMR (CD3OD): 1.66-1.75 (8H, m), 1.94-1.97 (6H, m), 2.05-2.07 (3H, m), 2.30 (2H, t, J=6.9 Hz), 3.08 (2H, q, J=6.9 Hz), 3.32 (2H, s); LC-MS (ESI) m/z calcd for C15H24N2O3 [M+H]+ 281.18. found [M+H]+ 281.25; mp 165 C. Anal. (C15H24N2O3) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476043B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-04fef6ade7b04310ac15b1c8322e858b |
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| Source note | uspto-grants-2013_07 |
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