HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038757Generated: October 31, 2026
tert-Butanol → Tert-butyl (1-(5-iodopyridin-2-YL)cyclobutyl)carbamate
https://huagongshe.com/reaction/2038757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 1-(5-Iodopyridin-2-YL)cyclobutanecarboxylic acid | HCID 67508444 | — |
| Product | Tert-butyl (1-(5-iodopyridin-2-YL)cyclobutyl)carbamate | HCID 67509277 | 22.8% |
Reaction Steps
1-(5-Iodo-pyridin-2-yl)-cyclobutane carboxylic acid (3.92 g, 12.9 mmol) was combined with tert-BuOH (6.1 mL, 65 mmol), Et3N (9.0 mL, 65 mmol) and DPPA (3.1 mL, 14 mmol). The reaction was heated to reflux (external bath: 85° C.) for 1.5 h. The volatiles were removed in vacuo and the crude reaction mixture was purified by normal phase flash chromatography on silica gel (5→80% EtOAc/hexanes) to give 1.1 g of [1-(5-iodo-pyridin-2-yl)-cyclobutyl]-carbamic acid tert-butyl ester as a solid, m/z 375.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575360B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-c546a4b2cd4b401f83ef17c80866eb45 |
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| Source note | uspto-grants-2013_11 |
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