HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645190Generated: November 1, 2026
Diisopropylethylamine → HCID 66775648, compound
https://huagongshe.com/reaction/1645190
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Methyl-1H-imidazole-4-carbonyl chloride hydrochloride | HCID 51341981 | — |
| Reactant | HCID 66775745 | HCID 66775745 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66775648 | HCID 66775648 | — |
Reaction Steps
To a stirring solution of 6-[(3-Trifluoromethoxy-benzylamino)-methyl]-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl ester prepared above (5.9 gm, 15.4 mmol) in 192 mL of CH3CN at room temperature under N2 was added DIEA (8.0 mL, 46.1 mmol) and 1-Methyl-1H-imidazole-4-carbonyl chloride HCL (5.6 gm, 30.7 mmol). After 24 hours, reaction was quenched with H2O, extracted with EtOAc. Organic layer was then washed with a 10% Citric acid solution, H2O, NaHCO3, and brine. The combined extracts were dried over anhydrous MgSO4, filtered and concentrated under reduced pressure, to yield 6.7 gm of 6-{[(1-Methyl-1H-imidazole-4-carbonyl)-(3-trifluoromethoxy-benzyl)-amino]-methyl}-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl ester 400 MHz 1H NMR (CDCl3) δ 7.8 (d, J=1.2 Hz, 1H), 7.3-7.1 (m, 5H), 5.4 (s, 1H), 4.8-4.7 (m, 1H), 4.2 (m, 1H), 3.7 (s, 1H), 3.7 (s, 3H), 3.4-3.2 (m, 3H), 1.4 (s, 9H), 1.3 (m, 2H), 0.8 (m, 1H); MS (M+1) 495.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124639B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-1ff8f7a451744044abad30b9f6cc7b82 |
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| Source note | uspto-grants-2012_02 |
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