HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885641Generated: October 27, 2026
Ethyl isothiocyanatoformate → Ethyl (6-bromo-pyridin-2-ylamino)carbonothioylcarbamate
https://huagongshe.com/reaction/885641
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl isothiocyanatoformate | HCID 85320 | — |
| Reactant | 2-Amino-6-bromopyridine | HCID 300809 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl (6-bromo-pyridin-2-ylamino)carbonothioylcarbamate | HCID 57361094 | — |
Reaction Steps
To a solution of 2-amino-6-bromopyridine (1) (253.8 g, 1.467 mol) in DCM (2.5 L) cooled to 5° C. is added ethoxycarbonyl isothiocyanate (173.0 mL, 1.467 mol) dropwise over 15 min. The reaction mixture is then allowed to warm to room temp. (20° C.) and stirred for 16 h. Evaporation in vacuo gives a solid which may be collected by filtration, thoroughly washed with petrol (3×600 mL) and air-dried to afford (2). The thiourea may be used as such for the next step without any purification. 1H (400 MHz, CDCl3) δ 12.03 (1H, br s, NH), 8.81 (1H, d, J 7.8 Hz, H-3), 8.15 (1H, br s, NH), 7.60 (1H, t, J 8.0 Hz, H-4), 7.32 (1H, dd, J 7.7 and 0.6 Hz, H-5), 4.31 (2H, q, J 7.1 Hz, CH2), 1.35 (3H, t, J 7.1 Hz, CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242274B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-bb3d62bca17b4bee91ad6323d55e5006 |
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| Source note | uspto-grants-2012_08 |
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